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nf-core/rnasplice nf-core/rnasplice

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Introduction

nf-core/rnasplice is a bioinformatics pipeline for alternative splicing analysis of RNA sequencing data obtained from organisms with a reference genome and annotation.

nf-core/rnasplice metro map

  1. Merge re-sequenced FastQ files (cat)
  2. Read QC (FastQC)
  3. Adapter and quality trimming (TrimGalore)
  4. Alignment with STAR
  5. Choice of quantification depending on analysis type:
    1. STAR -> Salmon
    2. STAR -> featureCounts
    3. STAR -> HTSeq (DEXSeq count)
  6. Sort and index alignments (SAMtools)
  7. Create bigWig coverage files (BEDTools, bedGraphToBigWig)
  8. Pseudo-alignment and quantification (Salmon; optional)
  9. Summarize QC (MultiQC)
  10. Differential Exon Usage (DEU):
    1. HTSeq -> DEXSeq
    2. featureCounts -> edgeR
    3. Quantification with featureCounts or HTSeq
    4. Differential exon usage with DEXSeq or edgeR
  11. Differential Transcript Usage (DTU):
    1. Salmon -> DRIMSeq -> DEXSeq
    2. Filtering with DRIMSeq
    3. Differential transcript usage with DEXSeq
  12. Event-based splicing analysis:
    1. STAR -> rMATS
    2. Salmon -> SUPPA2

Usage

Note

If you are new to Nextflow and nf-core, please refer to this page on how to set-up Nextflow. Make sure to test your setup with -profile test before running the workflow on actual data.

First, prepare a samplesheet with your input data that looks as follows:

samplesheet.csv:

sample,fastq_1,fastq_2,strandedness,condition
CONTROL_REP1,AEG588A1_S1_L002_R1_001.fastq.gz,AEG588A1_S1_L002_R2_001.fastq.gz,forward,CONTROL
CONTROL_REP1,AEG588A1_S1_L003_R1_001.fastq.gz,AEG588A1_S1_L003_R2_001.fastq.gz,forward,CONTROL
CONTROL_REP1,AEG588A1_S1_L004_R1_001.fastq.gz,AEG588A1_S1_L004_R2_001.fastq.gz,forward,CONTROL

Each row represents a fastq file (single-end) or a pair of fastq files (paired end). Rows with the same sample identifier are considered technical replicates and merged automatically. The strandedness refers to the library preparation and should be specified by the user.

:::warning Please provide pipeline parameters via the CLI or Nextflow -params-file option. Custom config files including those provided by the -c Nextflow option can be used to provide any configuration except for parameters; see docs. :::

Now, you can run the pipeline using:

nextflow run nf-core/rnasplice \
   --input samplesheet.csv \
   --contrasts contrastsheet.csv \
   --genome GRCh37 \
   --outdir <OUTDIR> \
   -profile <docker/singularity/.../institute>

Warning

Please provide pipeline parameters via the CLI or Nextflow -params-file option. Custom config files including those provided by the -c Nextflow option can be used to provide any configuration except for parameters; see docs.

For more details and further functionality, please refer to the usage documentation and the parameter documentation.

Pipeline output

To see the results of an example test run with a full size dataset refer to the results tab on the nf-core website pipeline page. For more details about the output files and reports, please refer to the output documentation.

Online videos

You can find numerous talks on the nf-core events page from various topics including writing pipelines/modules in Nextflow DSL2, using nf-core tooling, running nf-core pipelines as well as more generic content like contributing to Github. Please check them out!

Credits

nf-core/rnasplice was originally written by the bioinformatics team from Zifo RnD Solutions:

We thank Harshil Patel (@drpatelh) and Seqera Labs (seqeralabs) for their assistance in the development of this pipeline.

Zifo RnD Solutions

Contributions and Support

If you would like to contribute to this pipeline, please see the contributing guidelines.

For further information or help, don't hesitate to get in touch on the Slack #rnasplice channel (you can join with this invite).

Citations

If you use nf-core/rnasplice for your analysis, please cite it using the following doi: 10.5281/zenodo.8424632

An extensive list of references for the tools used by the pipeline can be found in the CITATIONS.md file.

You can cite the nf-core publication as follows:

The nf-core framework for community-curated bioinformatics pipelines.

Philip Ewels, Alexander Peltzer, Sven Fillinger, Harshil Patel, Johannes Alneberg, Andreas Wilm, Maxime Ulysse Garcia, Paolo Di Tommaso & Sven Nahnsen.

Nat Biotechnol. 2020 Feb 13. doi: 10.1038/s41587-020-0439-x.

rnasplice's People

Contributors

asmaali98 avatar bensouthgate avatar dkoppstein avatar jma1991 avatar keerthana-bhaskaran-tg avatar lathikaa avatar maxulysse avatar nf-core-bot avatar valentinoruggieri avatar

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rnasplice's Issues

The processes for splitting files are running very slowly with large numbers of input samples

Hello,

We are attempting to run this pipeline with a rather complex scenario: 850 contrasts and 3400 samples. The processes SPLIT_FILES_TPM, SPLIT_FILES_IOE and SPLIT_FILES_IOI appear to be running very slowly.

For example, looking at SPLIT_FILES_TPM, this has been running for 12 hours and only produced 61 TPM files so far. At this rate, it should take around 4 weeks to finish this process, before even attempting to run Suppa2...

We have successfully run these samples through nf-core/rnaseq (which took less than a week on 512 cores and 2 TB of RAM), and nf-core/differentialabundance (which only took 2 hours to run DESeq2). We now intend to run Suppa2 via this pipeline.

Any advice for speeding things up would be much appreciated. This is the command that we are running:

nextflow run nf-core/rnasplice -r 1.0.2 -c custom.config -params-file params.yml --igenomes_ignore --genome null \
--input /path/to/sample-sheet-rnasplice.csv \
--outdir run-rnasplice -profile docker --source salmon_results \
--fasta /path/to/genome/gencode_v45_spike-ins.fasta \
--gtf /path/to/genome/gencode_v45_spike-ins.gtf \
--star_index /path/to/genome/index/star \
--salmon_index /path/to/genome/index/salmon \
--dexseq_exon false --dexseq_dtu false \
--suppa --suppa_per_local_event \
--contrasts /path/to/contrasts-rnasplice.csv \
--sashimi_plot false

Missing rMATS arguments

Description of the bug

Not a bug as such, but more of a missing argument which is critical for rMATS.

one of the key rMATS arguments is libType (https://github.com/Xinglab/rmats-turbo?tab=readme-ov-file#all-arguments):

  --libType {fr-unstranded,fr-firststrand,fr-secondstrand}
                        Library type. Use fr-firststrand or fr-secondstrand
                        for strand-specific data. Only relevant to the prep
                        step, not the post step. Default: fr-unstranded

however in the rnasplice docs I don't see it exposed in the pipeline. Is is possible to choose the library type and I just missed?

Command used and terminal output

No response

Relevant files

No response

System information

No response

example contrastsheet.csv missing

Description of the bug

The link from the nf-core pipelines for the rnasplice contrastsheet: https://raw.githubusercontent.com/nf-core/rnasplice/dev/assets/contrastsheet.csv is blank, it looks like it was deleted from the github page under /dev/assets/ could someone re upload the correct contrast sheet, as this is the part of the pipeline I keep getting errors for.

Command used and terminal output

No response

Relevant files

No response

System information

No response

MISO error

Description of the bug

Event ENSG00000005302 not found in pickled directory index. Are you sure this is the right directory for the event?

Command used and terminal output

WARN: The operator `first` is useless when applied to a value channel which returns a single value by definition
ERROR ~ Error executing process > 'NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI (2)'

Caused by:
  Process `NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI (2)` terminated with an error exit status (1)

Command executed:

  sashimi_plot --plot-event ENSG00000005302 index miso_settings.txt --output-dir sashimi
  
  cat <<-END_VERSIONS > versions.yml
  "NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI":
      python: $(python --version | sed "s/Python //g")
      misopy: $(python -c "import pkg_resources; print(pkg_resources.get_distribution('misopy').version)")
  END_VERSIONS

Command exit status:
  1

Command output:
  (empty)

Command error:
  /usr/local/lib/python2.7/site-packages/matplotlib/cbook/deprecation.py:107: MatplotlibDeprecationWarning: The mpl_toolkits.axes_grid module was deprecated in version 2.1. Use mpl_toolkits.axes_grid1 and mpl_toolkits.axisartist provies the same functionality instead.
    warnings.warn(message, mplDeprecation, stacklevel=1)
  Traceback (most recent call last):
    File "/usr/local/bin/sashimi_plot", line 11, in <module>
      sys.exit(main())
    File "/usr/local/lib/python2.7/site-packages/misopy/sashimi_plot/sashimi_plot.py", line 276, in main
      plot_label=plot_label)
    File "/usr/local/lib/python2.7/site-packages/misopy/sashimi_plot/sashimi_plot.py", line 142, in plot_event
      %(event_name, pickle_dir)
  Exception: Event ENSG00000005302 not found in pickled directory index. Are you sure this is the right directory for the event?

Work dir:
  /flash/SciTechGrp/Zain/54/4ab0250756d10788d62592d4524e58

Tip: view the complete command output by changing to the process work dir and entering the command `cat .command.out`

 -- Check '.nextflow.log' file for details

Relevant files

No response

System information

No response

make contrasts file names consistent with those of the differentialabundance pipeline

Description of feature

Motivation

Many projects will use a combination of differentialabundance and rnasplice analysis, using as input the processed data from rnaseq. Thus keeping the workflows as consistent as possible would facilitate reusing files, for the user, and code, for developers.

Suggestion

The column names in the contrasts file are different from those of the differentialabundance pipeline. Would it possible to uniformize them?

in this pipeline contrast,treatment,control would becomes id,reference,target as in differentialabundance This would allow the re-use of the contrast file across the two nf-core pipelines for at least the simplest comparisons.

I am suggesting the change here because it seems to me that that differentialabundance is the more mature of the two and thus change there would result in more things breaking.

contrast file problem?

Description of the bug

I believe this could be a bug as I can't see any reason as far as I know for why this is not working.
image

The error is related to the contrast file (below attached). I also attached the samplesheet. csv

contrast.csv
samplesheet.csv

Command used and terminal output

nextflow run nf-core/rnasplice -r 1.0.1 -name NUTRIPROG1 -profile singularity -params-file nf-

params.json
{
    "input": ".\/samples\/samplesheet.csv",
    "contrasts": ".\/samples\/contrast.csv",
    "outdir": "\/uoa\/home\/r01mt19\/sharedscratch\/NUTRIPROG\/NUTRIPROG1_splice\/results",
    "email": "[email protected]",
    "multiqc_title": "NP1_MultiQC",
    "fasta": ".\/genome\/Salmo_salar.Ssal_v3.1.dna.toplevel.fa",
    "gtf": ".\/genome\/Salmo_salar.Ssal_v3.1.109.gtf",
    "aligner": "star_salmon",
    "rmats": true,
    "rmats_read_len": 2322889764,
    "dexseq_exon": true,
    "edger_exon": true,
    "dexseq_dtu": true
}

Relevant files

Jan-02 07:03:34.840 [Task submitter] DEBUG n.executor.local.LocalTaskHandler - Launch cmd line: /bin/bash -ue .command.run
Jan-02 07:03:34.841 [Task submitter] INFO nextflow.Session - [d9/23184d] Submitted process > NFCORE_RNASPLICE:RNASPLICE:INPUT_CHECK:SAMPLESHEET_CHECK (samplesheet.csv)
Jan-02 07:03:37.472 [Actor Thread 45] DEBUG nextflow.container.SingularityCache - Singularity pull complete image=https://depot.galaxyproject.org/singularity/gffread:0.12.1--h8b12597_0 path=/uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/singularity/depot.galaxyproject.org-singularity-gffread-0.12.1--h8b12597_0.img
Jan-02 07:03:37.497 [Task submitter] DEBUG n.executor.local.LocalTaskHandler - Launch cmd line: /bin/bash -ue .command.run
Jan-02 07:03:37.498 [Task submitter] INFO nextflow.Session - [d3/ed09de] Submitted process > NFCORE_RNASPLICE:RNASPLICE:TX2GENE_TXIMPORT_SALMON:GFFREAD_TX2GENE (Salmo_salar.Ssal_v3.1.109.gtf)
Jan-02 07:03:37.524 [Task submitter] DEBUG n.executor.local.LocalTaskHandler - Launch cmd line: /bin/bash -ue .command.run
Jan-02 07:03:37.525 [Task submitter] INFO nextflow.Session - [85/777fd2] Submitted process > NFCORE_RNASPLICE:RNASPLICE:TX2GENE_TXIMPORT_STAR_SALMON:GFFREAD_TX2GENE (Salmo_salar.Ssal_v3.1.109.gtf)
Jan-02 07:03:38.495 [Task monitor] DEBUG n.processor.TaskPollingMonitor - Task completed > TaskHandler[id: 1; name: NFCORE_RNASPLICE:RNASPLICE:CONTRASTS_CHECK:CONTRASTSHEET_CHECK (contrast.csv); status: COMPLETED; exit: 1; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/b3/1d2619589f656c58da4128c4fee2c6]
Jan-02 07:03:38.502 [Task monitor] DEBUG nextflow.processor.TaskProcessor - Handling unexpected condition for
task: name=NFCORE_RNASPLICE:RNASPLICE:CONTRASTS_CHECK:CONTRASTSHEET_CHECK (contrast.csv); work-dir=/uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/b3/1d2619589f656c58da4128c4fee2c6
error [nextflow.exception.ProcessFailedException]: Process NFCORE_RNASPLICE:RNASPLICE:CONTRASTS_CHECK:CONTRASTSHEET_CHECK (contrast.csv) terminated with an error exit status (1)
Jan-02 07:03:38.527 [Task monitor] ERROR nextflow.processor.TaskProcessor - Error executing process > 'NFCORE_RNASPLICE:RNASPLICE:CONTRASTS_CHECK:CONTRASTSHEET_CHECK (contrast.csv)'

Caused by:
Process NFCORE_RNASPLICE:RNASPLICE:CONTRASTS_CHECK:CONTRASTSHEET_CHECK (contrast.csv) terminated with an error exit status (1)

Command executed:

check_contrastsheet.py contrast.csv contrastsheet.valid.csv
cat <<-END_VERSIONS > versions.yml
"NFCORE_RNASPLICE:RNASPLICE:CONTRASTS_CHECK:CONTRASTSHEET_CHECK":
python: $(python --version | sed 's/Python //g')
END_VERSIONS

Command exit status:
1

Command output:
(empty)

Command error:
[CRITICAL] The contrast sheet must contain these column headers: control, treatment, contrast.

Work dir:
/uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/b3/1d2619589f656c58da4128c4fee2c6

Tip: you can try to figure out what's wrong by changing to the process work dir and showing the script file named .command.sh
Jan-02 07:03:38.548 [Task monitor] INFO nextflow.Session - Execution cancelled -- Finishing pending tasks before exit
Jan-02 07:03:38.558 [main] DEBUG nextflow.Session - Session await > all processes finished
Jan-02 07:03:38.598 [Actor Thread 59] DEBUG nextflow.processor.TaskProcessor - Handling unexpected condition for
task: name=NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; work-dir=null
error [java.lang.InterruptedException]: java.lang.InterruptedException
Jan-02 07:03:38.598 [Actor Thread 52] DEBUG nextflow.processor.TaskProcessor - Handling unexpected condition for
task: name=NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI; work-dir=null
error [java.lang.InterruptedException]: java.lang.InterruptedException
Jan-02 07:03:38.598 [Actor Thread 54] DEBUG nextflow.processor.TaskProcessor - Handling unexpected condition for
task: name=NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE; work-dir=null
error [java.lang.InterruptedException]: java.lang.InterruptedException
Jan-02 07:03:38.599 [Actor Thread 66] DEBUG nextflow.processor.TaskProcessor - Handling unexpected condition for
task: name=NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION; work-dir=null
error [java.lang.InterruptedException]: java.lang.InterruptedException
Jan-02 07:03:38.599 [Actor Thread 57] DEBUG nextflow.processor.TaskProcessor - Handling unexpected condition for
task: name=NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE; work-dir=null
error [java.lang.InterruptedException]: java.lang.InterruptedException
Jan-02 07:03:38.599 [Actor Thread 73] DEBUG nextflow.processor.TaskProcessor - Handling unexpected condition for
task: name=NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI; work-dir=null
error [java.lang.InterruptedException]: java.lang.InterruptedException
Jan-02 07:03:38.599 [Actor Thread 15] DEBUG nextflow.file.SortFileCollector - FileCollector temp dir not removed: null
Jan-02 07:03:38.622 [Actor Thread 46] DEBUG nextflow.file.SortFileCollector - FileCollector temp dir not removed: null
Jan-02 07:03:38.622 [Task monitor] DEBUG n.processor.TaskPollingMonitor - Task completed > TaskHandler[id: 2; name: NFCORE_RNASPLICE:RNASPLICE:INPUT_CHECK:SAMPLESHEET_CHECK (samplesheet.csv); status: COMPLETED; exit: 0; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/d9/23184d89571da1adf0b9d1b84fead3]
Jan-02 07:03:38.660 [Task monitor] DEBUG nextflow.util.ThreadPoolBuilder - Creating thread pool 'PublishDir' minSize=10; maxSize=240; workQueue=LinkedBlockingQueue[10000]; allowCoreThreadTimeout=false
Jan-02 07:03:49.495 [Task monitor] DEBUG n.processor.TaskPollingMonitor - Task completed > TaskHandler[id: 4; name: NFCORE_RNASPLICE:RNASPLICE:EDGER_DEU:SUBREAD_FLATTENGTF (Salmo_salar.Ssal_v3.1.109.gtf); status: COMPLETED; exit: 0; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/ca/b218a21cf5ad63f3b7a2ebe21baa16]
Jan-02 07:03:50.848 [Actor Thread 60] DEBUG nextflow.container.SingularityCache - Singularity pull complete image=https://depot.galaxyproject.org/singularity/gffread:0.12.7--hdcf5f25_3 path=/uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/singularity/depot.galaxyproject.org-singularity-gffread-0.12.7--hdcf5f25_3.img
Jan-02 07:03:53.447 [Task monitor] DEBUG n.processor.TaskPollingMonitor - Task completed > TaskHandler[id: 6; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:CUSTOM_GETCHROMSIZES (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: COMPLETED; exit: 0; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/f3/f45ec57c6bbf46ee01975e391ba395]
Jan-02 07:03:53.586 [Task monitor] DEBUG nextflow.processor.TaskProcessor - Process NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:CUSTOM_GETCHROMSIZES > Skipping output binding because one or more optional files are missing: fileoutparam<2:1>
Jan-02 07:04:12.536 [Task monitor] DEBUG n.processor.TaskPollingMonitor - Task completed > TaskHandler[id: 9; name: NFCORE_RNASPLICE:RNASPLICE:TX2GENE_TXIMPORT_STAR_SALMON:GFFREAD_TX2GENE (Salmo_salar.Ssal_v3.1.109.gtf); status: COMPLETED; exit: 0; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/85/777fd276623cca8d8517dd5778361b]
Jan-02 07:04:17.214 [Task monitor] DEBUG n.processor.TaskPollingMonitor - Task completed > TaskHandler[id: 12; name: NFCORE_RNASPLICE:RNASPLICE:TX2GENE_TXIMPORT_SALMON:GFFREAD_TX2GENE (Salmo_salar.Ssal_v3.1.109.gtf); status: COMPLETED; exit: 0; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/d3/ed09dedac6f08923075716649cb2a3]
Jan-02 07:07:49.055 [Actor Thread 49] DEBUG nextflow.container.SingularityCache - Singularity pull complete image=https://depot.galaxyproject.org/singularity/htseq:2.0.2--py310ha14a713_0 path=/uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/singularity/depot.galaxyproject.org-singularity-htseq-2.0.2--py310ha14a713_0.img
Jan-02 07:07:50.535 [Actor Thread 68] DEBUG nextflow.util.CacheHelper - Hash asset file sha-256: /uoa/home/r01mt19/.nextflow/assets/nf-core/rnasplice/bin/dexseq_prepare_annotation.py
Jan-02 07:08:10.323 [Task monitor] DEBUG n.processor.TaskPollingMonitor - Task completed > TaskHandler[id: 3; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:GTF_GENE_FILTER (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: COMPLETED; exit: 0; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/25/fd64ccb527636c0b5a95a48cb29b50]
Jan-02 07:08:30.524 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 07:08:51.849 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 2 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
Jan-02 07:13:30.544 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 07:13:51.924 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 2 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
Jan-02 07:18:30.558 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 07:18:52.161 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 2 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
Jan-02 07:19:16.853 [Actor Thread 44] DEBUG nextflow.container.SingularityCache - Singularity pull complete image=https://depot.galaxyproject.org/singularity/suppa:2.3--py36_0 path=/uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/singularity/depot.galaxyproject.org-singularity-suppa-2.3--py36_0.img
Jan-02 07:23:30.602 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 07:23:52.995 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 6 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
~> TaskHandler[id: 10; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/bf/41a0a46836f39bde096dc6392f5e27]
~> TaskHandler[id: 14; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/8d/f48e42145f5a63728ea2a7a6bb2f3d]
~> TaskHandler[id: 13; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/2a/100525ac82b2d516aacb8fc9b3a1c0]
~> TaskHandler[id: 11; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/84/134b660a04bcd3c2e75f3e7e725a1e]
Jan-02 07:28:30.642 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 07:28:53.907 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 6 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
~> TaskHandler[id: 10; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/bf/41a0a46836f39bde096dc6392f5e27]
~> TaskHandler[id: 14; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/8d/f48e42145f5a63728ea2a7a6bb2f3d]
~> TaskHandler[id: 13; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/2a/100525ac82b2d516aacb8fc9b3a1c0]
~> TaskHandler[id: 11; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/84/134b660a04bcd3c2e75f3e7e725a1e]
Jan-02 07:33:30.714 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 07:33:54.088 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 6 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
~> TaskHandler[id: 10; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/bf/41a0a46836f39bde096dc6392f5e27]
~> TaskHandler[id: 14; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/8d/f48e42145f5a63728ea2a7a6bb2f3d]
~> TaskHandler[id: 13; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/2a/100525ac82b2d516aacb8fc9b3a1c0]
~> TaskHandler[id: 11; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/84/134b660a04bcd3c2e75f3e7e725a1e]
Jan-02 07:38:30.742 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 07:38:54.867 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 6 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
~> TaskHandler[id: 10; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/bf/41a0a46836f39bde096dc6392f5e27]
~> TaskHandler[id: 14; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/8d/f48e42145f5a63728ea2a7a6bb2f3d]
~> TaskHandler[id: 13; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/2a/100525ac82b2d516aacb8fc9b3a1c0]
~> TaskHandler[id: 11; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/84/134b660a04bcd3c2e75f3e7e725a1e]
Jan-02 07:43:30.760 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 07:43:54.988 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 6 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
~> TaskHandler[id: 10; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/bf/41a0a46836f39bde096dc6392f5e27]
~> TaskHandler[id: 14; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/8d/f48e42145f5a63728ea2a7a6bb2f3d]
~> TaskHandler[id: 13; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/2a/100525ac82b2d516aacb8fc9b3a1c0]
~> TaskHandler[id: 11; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/84/134b660a04bcd3c2e75f3e7e725a1e]
Jan-02 07:48:30.764 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 07:48:55.235 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 6 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
~> TaskHandler[id: 10; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/bf/41a0a46836f39bde096dc6392f5e27]
~> TaskHandler[id: 14; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/8d/f48e42145f5a63728ea2a7a6bb2f3d]
~> TaskHandler[id: 13; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/2a/100525ac82b2d516aacb8fc9b3a1c0]
~> TaskHandler[id: 11; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/84/134b660a04bcd3c2e75f3e7e725a1e]
Jan-02 07:53:30.785 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 07:53:55.632 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 6 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
~> TaskHandler[id: 10; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/bf/41a0a46836f39bde096dc6392f5e27]
~> TaskHandler[id: 14; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/8d/f48e42145f5a63728ea2a7a6bb2f3d]
~> TaskHandler[id: 13; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/2a/100525ac82b2d516aacb8fc9b3a1c0]
~> TaskHandler[id: 11; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/84/134b660a04bcd3c2e75f3e7e725a1e]
Jan-02 07:58:30.875 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 07:58:56.483 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 6 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
~> TaskHandler[id: 10; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/bf/41a0a46836f39bde096dc6392f5e27]
~> TaskHandler[id: 14; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/8d/f48e42145f5a63728ea2a7a6bb2f3d]
~> TaskHandler[id: 13; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/2a/100525ac82b2d516aacb8fc9b3a1c0]
~> TaskHandler[id: 11; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/84/134b660a04bcd3c2e75f3e7e725a1e]
Jan-02 08:03:30.920 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 08:03:57.280 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 6 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
~> TaskHandler[id: 10; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/bf/41a0a46836f39bde096dc6392f5e27]
~> TaskHandler[id: 14; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/8d/f48e42145f5a63728ea2a7a6bb2f3d]
~> TaskHandler[id: 13; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/2a/100525ac82b2d516aacb8fc9b3a1c0]
~> TaskHandler[id: 11; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/84/134b660a04bcd3c2e75f3e7e725a1e]
Jan-02 08:08:30.937 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 08:08:57.344 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 6 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
~> TaskHandler[id: 10; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/bf/41a0a46836f39bde096dc6392f5e27]
~> TaskHandler[id: 14; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/8d/f48e42145f5a63728ea2a7a6bb2f3d]
~> TaskHandler[id: 13; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/2a/100525ac82b2d516aacb8fc9b3a1c0]
~> TaskHandler[id: 11; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/84/134b660a04bcd3c2e75f3e7e725a1e]
Jan-02 08:13:30.986 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 08:13:57.957 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 6 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
~> TaskHandler[id: 10; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/bf/41a0a46836f39bde096dc6392f5e27]
~> TaskHandler[id: 14; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/8d/f48e42145f5a63728ea2a7a6bb2f3d]
~> TaskHandler[id: 13; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/2a/100525ac82b2d516aacb8fc9b3a1c0]
~> TaskHandler[id: 11; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/84/134b660a04bcd3c2e75f3e7e725a1e]
Jan-02 08:18:31.027 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 08:18:58.269 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 6 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
~> TaskHandler[id: 10; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/bf/41a0a46836f39bde096dc6392f5e27]
~> TaskHandler[id: 14; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/8d/f48e42145f5a63728ea2a7a6bb2f3d]
~> TaskHandler[id: 13; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/2a/100525ac82b2d516aacb8fc9b3a1c0]
~> TaskHandler[id: 11; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/84/134b660a04bcd3c2e75f3e7e725a1e]
Jan-02 08:23:31.086 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 08:23:59.155 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 6 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
~> TaskHandler[id: 10; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/bf/41a0a46836f39bde096dc6392f5e27]
~> TaskHandler[id: 14; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/8d/f48e42145f5a63728ea2a7a6bb2f3d]
~> TaskHandler[id: 13; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/2a/100525ac82b2d516aacb8fc9b3a1c0]
~> TaskHandler[id: 11; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/84/134b660a04bcd3c2e75f3e7e725a1e]
Jan-02 08:28:31.088 [Task monitor] DEBUG n.processor.TaskPollingMonitor - !! executor local > tasks to be completed: 1 -- submitted tasks are shown below
~> TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: RUNNING; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 08:28:44.984 [Task monitor] DEBUG n.processor.TaskPollingMonitor - Task completed > TaskHandler[id: 5; name: NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:STAR_GENOMEGENERATE (Salmo_salar.Ssal_v3.1.dna.toplevel.fa); status: COMPLETED; exit: 0; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/91/54dc6a038f8be4c73d798b925c52d6]
Jan-02 08:28:46.453 [Task monitor] DEBUG n.processor.TaskPollingMonitor - <<< barrier arrives (monitor: local) - terminating tasks monitor poll loop
Jan-02 08:28:46.656 [main] DEBUG nextflow.Session - Session await > all barriers passed
Jan-02 08:28:46.816 [main] DEBUG nextflow.util.ThreadPoolManager - Thread pool 'PublishDir' shutdown completed (hard=false)
Jan-02 08:28:50.996 [main] INFO nextflow.Nextflow - -�[0;35m[nf-core/rnasplice]�[0;32m Sent summary e-mail to [email protected] (sendmail)-
Jan-02 08:28:52.105 [main] INFO nextflow.Nextflow - -�[0;35m[nf-core/rnasplice]�[0;31m Pipeline completed with errors�[0m-
Jan-02 08:28:56.672 [main] DEBUG n.trace.WorkflowStatsObserver - Workflow completed > WorkflowStats[succeededCount=7; failedCount=1; ignoredCount=0; cachedCount=0; pendingCount=6; submittedCount=0; runningCount=0; retriesCount=0; abortedCount=0; succeedDuration=17h 6m 32s; failedDuration=3.6s; cachedDuration=0ms;loadCpus=0; loadMemory=0; peakRunning=8; peakCpus=21; peakMemory=114 GB; ]
Jan-02 08:28:56.673 [main] DEBUG nextflow.trace.TraceFileObserver - Workflow completed -- saving trace file
Jan-02 08:28:56.715 [main] DEBUG nextflow.trace.ReportObserver - Workflow completed -- rendering execution report
Jan-02 08:28:59.488 [Task submitter] DEBUG n.processor.TaskPollingMonitor - %% executor local > tasks in the submission queue: 6 -- tasks to be submitted are shown below
~> TaskHandler[id: 8; name: NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3; status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/1a/89621de8f0a100a313ae6c641a01c5]
~> TaskHandler[id: 7; name: NFCORE_RNASPLICE:RNASPLICE:DEXSEQ_DEU:DEXSEQ_ANNOTATION (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/6c/c1922f429ef61c8742847108caf556]
~> TaskHandler[id: 10; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/bf/41a0a46836f39bde096dc6392f5e27]
~> TaskHandler[id: 14; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/8d/f48e42145f5a63728ea2a7a6bb2f3d]
~> TaskHandler[id: 13; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:GENERATE_EVENTS_IOE (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/2a/100525ac82b2d516aacb8fc9b3a1c0]
~> TaskHandler[id: 11; name: NFCORE_RNASPLICE:RNASPLICE:SUPPA_STAR_SALMON:GENERATE_EVENTS_IOI (Salmo_salar.Ssal_v3.1.109.gtf); status: NEW; exit: -; error: -; workDir: /uoa/scratch/users/r01mt19/NUTRIPROG/NUTRIPROG1_splice/work/84/134b660a04bcd3c2e75f3e7e725a1e]
Jan-02 08:29:15.669 [main] DEBUG nextflow.trace.TimelineObserver - Workflow completed -- rendering execution timeline
Jan-02 08:29:18.993 [main] DEBUG nextflow.cache.CacheDB - Closing CacheDB done
Jan-02 08:29:18.994 [main] INFO org.pf4j.AbstractPluginManager - Stop plugin '[email protected]'
Jan-02 08:29:18.995 [main] DEBUG nextflow.plugin.BasePlugin - Plugin stopped nf-validation
Jan-02 08:29:19.249 [main] DEBUG nextflow.util.ThreadPoolManager - Thread pool 'FileTransfer' shutdown completed (hard=false)
Jan-02 08:29:19.501 [main] DEBUG nextflow.script.ScriptRunner - > Execution complete -- Goodbye

System information

HPC - slurm - singularity
nextflow/23.10.0
nf-core/rnasplice -r 1.0.1

The pipeline should be able to infer strandedness from FASTQ (i.e. allow "auto" for strandedness in the CSV)

Description of feature

When running the pipeline from FASTQ files, the user currently needs to specify the strandedness as one of unstranded, forward or reverse, according to the documentation: https://nf-co.re/rnasplice/dev/docs/usage#samplesheet-input

It would be great to allow users to set this to auto and have the pipeline be able to infer strandedness automatically, the way nf-core/rnaseq does.

DRIMSEQ_FILTER error

Description of the bug

Dear All, I am testing the pipeline and I am facing the following error,
Not all conditions are included in the contrast file.
Thanks for your support

Error executing process > 'NFCORE_RNASPLICE:RNASPLICE:DRIMSEQ_DEXSEQ_DTU_SALMON:DRIMSEQ_FILTER (1)'

Caused by:
  Process `NFCORE_RNASPLICE:RNASPLICE:DRIMSEQ_DEXSEQ_DTU_SALMON:DRIMSEQ_FILTER (1)` terminated with an error exit status (1)

Command executed:

  run_drimseq_filter.R salmon.merged.txi.dtu.rds q.tx2gene.tsv samplesheet.csv \
      4 \
      2 \
      2 \
      10 \
      0.1 \
      10
  
  cat <<-END_VERSIONS > versions.yml
  "NFCORE_RNASPLICE:RNASPLICE:DRIMSEQ_DEXSEQ_DTU_SALMON:DRIMSEQ_FILTER":
      r-base: $(echo $(R --version 2>&1) | sed 's/^.*R version //; s/ .*$//')
      bioconductor-drimseq: $(Rscript -e "library(DRIMSeq); cat(as.character(packageVersion('DRIMSeq')))")
  END_VERSIONS

Command exit status:
  1

Command output:
  (empty)

Command error:
  
  Attaching package: 'DRIMSeq'
  
  The following object is masked from 'package:base':
  
      proportions
  
  Error in .local(x, ...) : 
    min_samps_gene_expr >= 0 && min_samps_gene_expr <= ncol(x@counts) is not TRUE
  Calls: <Anonymous> -> <Anonymous> -> .local -> stopifnot
  Execution halted

Command used and terminal output

nextflow run nf-core/rnasplice --input $wd/samplesheet.csv \
							   --contrasts $wd/contrast.csv \
							   --outdir test \
							   --genome GRCm38 \
							   -profile singularity \
							   --aligner star \
							   --dexseq_exon \
							   --edger_exon \
							   --rmats \
							   --rmats_read_len 75 \
							   --save_reference true \
							   --sashimi_plot true \
							   -config config.config \
							   -r dev

Relevant files

nextflow.log

System information

nextflow/22.10.4
HPC - slurm
Operating System: Debian GNU/Linux 10 (buster)

DEXSeq-DTU Stager pScreenAdjusted

Description of the bug

I have a question regarding a parameter in the stager screening procedure:
/bin/run_stager.R
line 147:

object <- stageRTx(
    pScreen         = output[["pScreen"]],
    pConfirmation   = output[["pConfirmation"]],
    tx2gene         = output[["tx2gene"]],
    pScreenAdjusted = FALSE
)

Why is pScreenAdjusted set to FALSE, I thought that the perGeneQvalue outputed by DEXseq is already adjusted, as described by the function helper in DEXSeq, which would mean the parameter should be set to TRUE here. This is also set to TRUE in the original workflow proposed in:
https://f1000research.com/articles/7-952/v3

MISO_SASHIMI step fails when using scratch directory

Description of the bug

When using the process$scratch variable in the configuration file, NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI fails by looking in the scratch directory instead of where the pickle files actually are. Here, process$scratch is set to $TMPDIR, which gets expanded to /local/xxxxx/20738687/cluster_tmp.

However, then MISO fails with:

Exception: Error: no filename /local/xxxxx/20738687/cluster_tmp/nxf.R4ElqFeq2j/index/chrX/ENSG00000004961.pickle

The pickle files are however actually in the output directory, not the scratch directory:

(base) -bash-4.2$ find test2 -name *.pickle | head
test2/misopy/index/chrX/ENSG00000130962.pickle
test2/misopy/index/chrX/ENSG00000126952.pickle
test2/misopy/index/chrX/ENSG00000242013.pickle
test2/misopy/index/chrX/ENSG00000196632.pickle
test2/misopy/index/chrX/ENSG00000130830.pickle
test2/misopy/index/chrX/ENSG00000184033.pickle
test2/misopy/index/chrX/ENSG00000101892.pickle
test2/misopy/index/chrX/ENSG00000133149.pickle
test2/misopy/index/chrX/ENSG00000165194.pickle
test2/misopy/index/chrX/ENSG00000198689.pickle

Full error:

-[nf-core/rnasplice] Pipeline completed with errors-
ERROR ~ Error executing process > 'NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI (1)'

Caused by:
  Process `NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI (1)` terminated with an error exit status (1)

Command executed:

  sashimi_plot --plot-event ENSG00000004961 index miso_settings.txt --output-dir sashimi

  cat <<-END_VERSIONS > versions.yml
  "NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI":
      python: $(python --version | sed "s/Python //g")
      misopy: $(python -c "import pkg_resources; print(pkg_resources.get_distribution('misopy').version)")
  END_VERSIONS

Command exit status:
  1

Command output:
  (empty)

Command error:
  WARNING: DEPRECATED USAGE: Forwarding SINGULARITYENV_TMPDIR as environment variable will not be supported in the future, use APPTAINERENV_TMPDIR instead
  WARNING: DEPRECATED USAGE: Forwarding SINGULARITYENV_NXF_DEBUG as environment variable will not be supported in the future, use APPTAINERENV_NXF_DEBUG instead
  /usr/local/lib/python2.7/site-packages/matplotlib/cbook/deprecation.py:107: MatplotlibDeprecationWarning: The mpl_toolkits.axes_grid module was deprecated in version 2.1. Use mpl_toolkits.axes_grid1 and mpl_toolkits.axisartist provies the same functionality instead.
    warnings.warn(message, mplDeprecation, stacklevel=1)
  Traceback (most recent call last):
    File "/usr/local/bin/sashimi_plot", line 11, in <module>
      sys.exit(main())
    File "/usr/local/lib/python2.7/site-packages/misopy/sashimi_plot/sashimi_plot.py", line 276, in main
      plot_label=plot_label)
    File "/usr/local/lib/python2.7/site-packages/misopy/sashimi_plot/sashimi_plot.py", line 153, in plot_event
      plot_label=plot_label)
    File "/usr/local/lib/python2.7/site-packages/misopy/sashimi_plot/plot_utils/plot_gene.py", line 675, in plot_density_from_file
      parseGene(pickle_filename, event)
    File "/usr/local/lib/python2.7/site-packages/misopy/parse_gene.py", line 11, in parseGene
      raise Exception, "Error: no filename %s" %(pickle_filename)
  Exception: Error: no filename /local/xxxxx/20738687/cluster_tmp/nxf.R4ElqFeq2j/index/chrX/ENSG00000004961.pickle

Command used and terminal output

nextflow run nf-core/rnasplice -profile test -c dkfz.config --outdir test2 -r dev

Relevant files

dkfz.config

params {
    config_profile_description = 'Deutsches Krebsforschungszentrum (DKFZ) HPC cluster profile provided by nf-core/configs'
    config_profile_contact     = 'Kübra Narcı [email protected]'
    config_profile_name        = 'DKFZ cluster'


    max_cpus   = 30
    max_memory = '250.GB'
    max_time   = '48.h'
}


singularity {
  enabled = true
  autoMounts = true
}

process {
  executor = 'lsf'
  clusterOptions = '-L /bin/bash'
  scratch = '$TMPDIR'
}

executor {
  name = 'lsf'
  perTaskReserve = false
  perJobMemLimit = true
  queueSize = 10
  submitRateLimit = '3 sec'
}

System information

  • Nextflow version: 23.04.1 build 5866
  • Hardware: HPC (LSF)
  • Executor: 'lsf'
  • Container engine: Singularity
  • OS: CentOS Linux 7
  • Version of nf-core/rnasplice: dev

Error with rmats.py when running with multiple contrasts: <filename>.bam not found in .rmats files

Description of the bug

Running the pipeline with multiple contrasts in the contrast sheet results in multiple errors as mentioned in the filename. The pipeline runs fine with only one contrast at a time. As such, it's possible that this issue might be related to a separate report, which was focused on SUPPA: #71

Relevant input files, as well as the full log, are attached below.

Command used and terminal output

nextflow run nf-core/rnasplice -r dev -latest -c custom.config -params-file params.yml --igenomes_ignore --genome null \
--input /data/share/santina-cutrupi/sample-sheet-rnasplice.csv \
--outdir test-rnasplice -profile docker --source genome_bam \
--fasta /data/share/santina-cutrupi/genome/gencode_v44_spike-ins.fasta \
--gtf /data/share/santina-cutrupi/genome/gencode_v44_spike-ins.gtf \
--star_index /data/share/santina-cutrupi/genome/index/star \
--salmon_index /data/share/santina-cutrupi/genome/index/salmon \
--rmats --rmats_read_len 100 --rmats_paired_stats \
--contrasts /data/share/santina-cutrupi/contrasts-rnasplice.csv \
--aligner star --dexseq_exon false --miso_genes "ENSG00000004961.15, ENSG00000005302.19, ENSG00000147403.18"



-[nf-core/rnasplice] Pipeline completed with errors-
ERROR ~ Error executing process > 'NFCORE_RNASPLICE:RNASPLICE:RMATS:RMATS_POST (HepG2_TARDBP_TRT-HepG2_TARDBP_CTL)'

Caused by:
  Process `NFCORE_RNASPLICE:RNASPLICE:RMATS:RMATS_POST (HepG2_TARDBP_TRT-HepG2_TARDBP_CTL)` terminated with an error exit status (1)

Command executed:

  mkdir -p HepG2_TARDBP_TRT-HepG2_TARDBP_CTL/rmats_post
  
  rmats.py \
      --gtf gencode_v44_spike-ins.gtf \
      --b1 HepG2_TARDBP_TRT_bamlist.txt \
      --b2 HepG2_TARDBP_CTL_bamlist.txt \
      --od HepG2_TARDBP_TRT-HepG2_TARDBP_CTL/rmats_post \
      --tmp HepG2_TARDBP_TRT-HepG2_TARDBP_CTL/rmats_temp \
      -t paired \
      --libType fr-unstranded \
      --readLength 100 \
      --variable-read-length \
      --nthread 12 \
      --tstat 12 \
      --cstat 0.0001 \
      --task post \
      --paired-stats \
       \
       \
       \
      --allow-clipping \
      1> HepG2_TARDBP_TRT-HepG2_TARDBP_CTL/rmats_post.log
  
  cat <<-END_VERSIONS > versions.yml
  "NFCORE_RNASPLICE:RNASPLICE:RMATS:RMATS_POST":
      rmats: $(echo $(rmats.py --version) | sed -e "s/v//g")
  END_VERSIONS

Command exit status:
  1

Command output:
  (empty)

Command error:
  HepG2_TARDBP_TRT_REP2_sorted.bam not found in .rmats files
  HepG2_TARDBP_TRT_REP1_sorted.bam not found in .rmats files
  HepG2_TARDBP_CTL_REP1_sorted.bam not found in .rmats files
  HepG2_TARDBP_CTL_REP2_sorted.bam not found in .rmats files

Work dir:
  /data/share/santina-cutrupi/work/44/1986fadc43abab0d325223ec214ee9

Tip: you can try to figure out what's wrong by changing to the process work dir and showing the script file named `.command.sh`

 -- Check '.nextflow.log' file for details

Relevant files

custom.config.txt
params.yml.txt
contrasts-rnasplice.csv.txt
sample-sheet-rnasplice.csv.txt
nextflow.log.txt

System information

Nextflow 23.04.2
Latest Dev version of the rnasplice pipeline

dexseq: stager.R: subscript out of bounds.

Description of the bug

Hey all, I had a package error: 'stager.R: subscript out of bounds.' when I was running rnasplice pipeline, it seems like stage-wise adjustment out of range in gene expression process. I'd be so thankful if anyone could provide some advices:

Command used and terminal output

nextflow run nf-core/rnasplice --input --outdir  -r dev --skip_alignment false  --rmats true --dexseq_exon true --edger_exon true --dexseq_dtu true-profile singularity --

Relevant files

INFO: Converting SIF file to temporary sandbox...
WARNING: Skipping mount /home/yl/.conda/envs/nf-core/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container
Loading required package: SummarizedExperiment
Loading required package: MatrixGenerics
Loading required package: matrixStats
Attaching package: 'MatrixGenerics'
The following objects are masked from 'package:matrixStats':
colAlls, colAnyNAs, colAnys, colAvgsPerRowSet, colCollapse,
colCounts, colCummaxs, colCummins, colCumprods, colCumsums,
colDiffs, colIQRDiffs, colIQRs, colLogSumExps, colMadDiffs,
colMads, colMaxs, colMeans2, colMedians, colMins, colOrderStats,
colProds, colQuantiles, colRanges, colRanks, colSdDiffs, colSds,
colSums2, colTabulates, colVarDiffs, colVars, colWeightedMads,
colWeightedMeans, colWeightedMedians, colWeightedSds,
colWeightedVars, rowAlls, rowAnyNAs, rowAnys, rowAvgsPerColSet,
rowCollapse, rowCounts, rowCummaxs, rowCummins, rowCumprods,
rowCumsums, rowDiffs, rowIQRDiffs, rowIQRs, rowLogSumExps,
rowMadDiffs, rowMads, rowMaxs, rowMeans2, rowMedians, rowMins,
rowOrderStats, rowProds, rowQuantiles, rowRanges, rowRanks,
rowSdDiffs, rowSds, rowSums2, rowTabulates, rowVarDiffs, rowVars,
rowWeightedMads, rowWeightedMeans, rowWeightedMedians,
rowWeightedSds, rowWeightedVars
Loading required package: GenomicRanges
Loading required package: stats4
Loading required package: BiocGenerics
Loading required package: parallel
Attaching package: 'BiocGenerics'
The following objects are masked from 'package:parallel':
clusterApply, clusterApplyLB, clusterCall, clusterEvalQ,
clusterExport, clusterMap, parApply, parCapply, parLapply,
parLapplyLB, parRapply, parSapply, parSapplyLB
The following objects are masked from 'package:stats':
IQR, mad, sd, var, xtabs
The following objects are masked from 'package:base':
Filter, Find, Map, Position, Reduce, anyDuplicated, append,
as.data.frame, basename, cbind, colnames, dirname, do.call,
duplicated, eval, evalq, get, grep, grepl, intersect, is.unsorted,
lapply, mapply, match, mget, order, paste, pmax, pmax.int, pmin,
pmin.int, rank, rbind, rownames, sapply, setdiff, sort, table,
tapply, union, unique, unsplit, which.max, which.min
Loading required package: S4Vectors
Attaching package: 'S4Vectors'
The following object is masked from 'package:base':
expand.grid
Loading required package: IRanges
Loading required package: GenomeInfoDb
Loading required package: Biobase
Welcome to Bioconductor
Vignettes contain introductory material; view with
'browseVignettes()'. To cite Bioconductor, see
'citation("Biobase")', and for packages 'citation("pkgname")'.
Attaching package: 'Biobase'
The following object is masked from 'package:MatrixGenerics':
rowMedians
The following objects are masked from 'package:matrixStats':
anyMissing, rowMedians
Attaching package: 'stageR'
The following object is masked from 'package:methods':
getMethod
Error in [<-(*tmp*, idCon, 1, value = unlist(txLevelAdjustments)) :
subscript out of bounds
Calls: stageWiseAdjustment -> stageWiseAdjustment -> .local -> .stageWiseTest
Execution halted
INFO: Cleaning up image...

System information

Nextflow version (22.10.1)
256 cores 280GB
singularity
ubuntu 22.04
-r dev

Empty output for BAM+rMats

Description of the bug

Hi, I passed the test samples. But when I run on my samples (BAM+rMats). I got empty rMats output. There was no error reported, showing completed.

Command used and terminal output

$ nextflow run software/rnasplice -profile docker --input nf_samplesheet.csv --contrasts nf_contrastsheet.csv --genome GRCh38 --outdir myenv

Relevant files

nextflow.log
nextflow.config.log

System information

No response

check_contrastsheet not identifying headers even though they're present

I ran the pipeline through Tower and it keeps kicking back the error of my contrast sheet having no header. I ran just the checkcontrastsheet.py locally on the csv and it's giving the same error. It doesn't happen on Tower when I run it with the test data though. Not sure what to make of this. I'm just including the python I ran locally before because it 100% recapitulates the issue without having to run the whole pipeline.

ejennings@DESKTOP-C17P9CF Downloads % python check_contrastsheet.py contrast_test_share.csv testout
[CRITICAL] The given contrast sheet does not appear to contain a header.

This is the CSV I tested on:
contrast_test_share.csv

test profile: miso_index failure

Description of the bug

MISO_INDEX runs and appears to create an output file "/index/genes.gff" (according to command.log), but the pipeline breaks with the below error.
Upon checking the work directory, there is only the log files; no ".gff".

Command used and terminal output

nextflow -c nextflow.config run nf-core/rnasplice -r dev -
profile test --outdir 's3://mdibl-jhfuqua/'

Aug-22 14:15:28.171 [Task monitor] ERROR nextflow.processor.TaskProcessor - Error executing process > 'NFCORE_RNASPLIC
E:RNASPLICE:VISUALISE_MISO:MISO_INDEX'

Caused by:
  Missing output file(s) `index` expected by process `NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_INDEX`

Command executed:

  index_gff --index genes_chrX_genes.gff3 index

  cat <<-END_VERSIONS > versions.yml
  "NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_INDEX":
      python: $(python --version | sed "s/Python //g")
      misopy: $(python -c "import pkg_resources; print(pkg_resources.get_distribution('misopy').version)")
  END_VERSIONS

Command exit status:
  0

Command output:
  (empty)

Relevant files

nextflow.log
command-2.log

System information

No response

DRIMSEQ_FILTER error

Description of the bug

I am running rnasplice using the STAR mapping, and Salmon output files from the nf-core rnaseq pipeline. I presume, if I implement this in the nf-params file, rnaplice can work with the rnaseq output. I am getting the following error:

Command error:
  INFO:    Converting SIF file to temporary sandbox...
  WARNING: Skipping mount /home/lety/data/CBBI_Projects/general/software/miniconda3/var/singularity/mnt/session/etc/resolv.conf [files]: /etc/resolv.conf doesn't exist in container

  Attaching package: 'DRIMSeq'

  The following object is masked from 'package:base':

      proportions

  Error in .local(x, ...) :
    min_samps_gene_expr >= 0 && min_samps_gene_expr <= ncol(x@counts) is not TRUE
  Calls: <Anonymous> -> <Anonymous> -> .local -> stopifnot
  Execution halted
  INFO:    Cleaning up image...

This is a similar error to the closed issue #69
Where running this pipeline through conda or docker solved the problem. However, I can not deviate from using singularity. Are there other options to solve this error?
A commenter suggested that this is a known STAR 2.7.10a issue.
How can we proceed with this issue?

Command used and terminal output

nextflow \
	run nf-core/rnasplice \
	-r 1.0.0 \
	-profile singularity \
	--singularity_pull_docker_container \
	-name $runname \
	-params-file nf-params_rnasplice.json \
	-resume

Relevant files

parameter file:

{
  "fasta": "/data/CBBI_Projects/SNRPA_Function/processed/dgrashof/snrpa_function/dgrashof/Nextflow/RNAseq_Salmon/genomes/GRCm39.primary_assembly.genome.fa",
  "gtf": "/data/CBBI_Projects/SNRPA_Function/processed/dgrashof/snrpa_function/dgrashof/Nextflow/RNAseq_Salmon/genomes/gencode.vM28.primary_assembly.annotation.gtf",
  "gencode": true,
  "save_reference": true,
  "save_unaligned": true,
  "save_align_intermeds": true,
  "aligner": "star_salmon",
  "extra_salmon_quant_args": "--incompatPrior 0.0",
  "max_cpus": 30,
  "skip_trimming": false,
  "trim_nextseq": 25,
  "deseq2_vst": true,
  "max_memory": "60.GB",
  "max_time": "168h",
  "save_trimmed": true,
  "pseudo_aligner": "salmon",
  "skip_bigwig": false,
  "skip_preseq": false,
  "skip_qualimap": false,
  "skip_dupradar": false,
  "skip_biotype_qc": false,
  "skip_markduplicates": false,
  "rseqc_modules": "bam_stat,inner_distance,infer_experiment,junction_annotation,junction_saturation,read_distribution,read_duplication,tin"
}

System information

No response

ERROR ~ No such variable: Exception evaluating property 'out' for nextflow.script.ChannelOut

Description of the bug

Hello,

I'm getting the error from the title when testing the pipeline, starting from BAM files produced by nf-core/rnaseq. Tested with the latest dev version and Nextflow 23.04.0. This the the output:

------------------------------------------------------
[-        ] process > NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:GUNZIP_GTF             -
[-        ] process > NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:GTF_GENE_FILTER        -
[-        ] process > NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:MAKE_TRANSCRIPTS_FASTA -
[-        ] process > NFCORE_RNASPLICE:RNASPLICE:PREPARE_GENOME:CUSTOM_GETCHROMSIZES   -
ERROR ~ No such variable: Exception evaluating property 'out' for nextflow.script.ChannelOut, Reason: groovy.lang.MissingPropertyException: No such property: out for class: groovyx.gpars.dataflow.DataflowBroadcast

 -- Check script '/data/share/.nextflow/assets/nf-core/rnasplice/./workflows/rnasplice.nf' at line: 175 or see '.nextflow.log' file for more details

The last printed message seems to refer to this part of the code: https://github.com/nf-core/rnasplice/blob/dev/workflows/rnasplice.nf#L175-L179

I am attaching the full log below.

Command used and terminal output

No response

Relevant files

nextflow.log

System information

No response

STAGER error: subscript out of bounds

Description of the bug

As referenced here #83

I am still stopped at this point:

run_stager.R CP_TG-CP_WT DEXSeqResults.CP_TG-CP_WT.tsv perGeneQValue.CP_TG-CP_WT.tsv dexseq

Error in[<-(tmp, idCon, 1, value = unlist(txLevelAdjustments)) : subscript out of bounds Calls: stageWiseAdjustment -> stageWiseAdjustment -> .local -> .stageWiseTest Execution halted

Any suggestion?
Best

Command used and terminal output

nextflow run nf-core/rnasplice --input $wd/samplesheet_orig.csv \
						--contrasts $wd/contrast.csv \
						--outdir splice_Brain_TG_vs_Brain_WT \
						--genome GRCm38 \
						--aligner star_salmon \
							--dexseq_exon true \
							--min_samps_gene_expr 2 \
							--min_samps_feature_expr 2 \
							--min_gene_expr 5 \
							   --min_feature_expr 5 \
							   --min_feature_prop 0.2 \
							   --edger_exon true\
							   --rmats false \
							   --dexseq_dtu true \
							   --suppa true \
							   --suppa_per_local_event true \
							   --suppa_per_isoform true \
							   --save_reference true \
							   --sashimi_plot false \
							   -config $wd/config_HPC.config \
							   -profile docker \
							   -r dev

Relevant files

contrast.csv
nextflow.log
splicing_P107535352.log

System information

N E X T F L O W ~ version 23.04.2
Launching https://github.com/nf-core/rnasplice [hopeful_gilbert] DSL2 - revision: 9fe10b0 [dev]
Debian 10

STAGER error: subscript out of bounds

Description of the bug

Dear All,
As anticipated here, #71, I am now facing an issue with run_stager command. Here are relevant info. Many thks

run_stager.R CP-Brain DEXSeqResults.CP-Brain.tsv perGeneQValue.CP-Brain.tsv dexseq

Command used and terminal output

nextflow run nf-core/rnasplice --input $wd/samplesheet.csv \
							   --contrasts $wd/contrast.csv \
							   --outdir splice_attempt1 \
							   --genome GRCm38 \
							   --aligner star \
							   --min_samps_gene_expr 2 \
							   --min_samps_feature_expr 2 \
							   --min_gene_expr 5 \
							   --min_feature_expr 5 \
							   --min_feature_prop 0.2 \
							   --dexseq_exon true \
							   --edger_exon true\
							   --rmats true \
							   --rmats_read_len 75 \
							   --save_reference true \
							   --sashimi_plot true \
							   -config config.config \
							   -profile docker \
							   -r dev
exit 0




ERROR ~ Error executing process > 'NFCORE_RNASPLICE:RNASPLICE:DRIMSEQ_DEXSEQ_DTU_SALMON:STAGER (1)'

Caused by:
  Process `NFCORE_RNASPLICE:RNASPLICE:DRIMSEQ_DEXSEQ_DTU_SALMON:STAGER (1)` terminated with an error exit status (1)

Command executed:

  run_stager.R CP-Brain DEXSeqResults.CP-Brain.tsv perGeneQValue.CP-Brain.tsv dexseq
  
  cat <<-END_VERSIONS > versions.yml
  "NFCORE_RNASPLICE:RNASPLICE:DRIMSEQ_DEXSEQ_DTU_SALMON:STAGER":
      r-base: $(echo $(R --version 2>&1) | sed 's/^.*R version //; s/ .*$//')
      bioconductor-stager: $(Rscript -e "library(stageR); cat(as.character(packageVersion('stageR')))")
  END_VERSIONS

Command exit status:
  1

Command output:
  (empty)

Command error:
      IQR, mad, sd, var, xtabs
  
  The following objects are masked from 'package:base':
  
      Filter, Find, Map, Position, Reduce, anyDuplicated, append,
      as.data.frame, basename, cbind, colnames, dirname, do.call,
      duplicated, eval, evalq, get, grep, grepl, intersect, is.unsorted,
      lapply, mapply, match, mget, order, paste, pmax, pmax.int, pmin,
      pmin.int, rank, rbind, rownames, sapply, setdiff, sort, table,
      tapply, union, unique, unsplit, which.max, which.min
  
  Loading required package: S4Vectors
  
  Attaching package: 'S4Vectors'
  
  The following object is masked from 'package:base':
  
      expand.grid
  
  Loading required package: IRanges
  Loading required package: GenomeInfoDb
  Loading required package: Biobase
  Welcome to Bioconductor
  
      Vignettes contain introductory material; view with
      'browseVignettes()'. To cite Bioconductor, see
      'citation("Biobase")', and for packages 'citation("pkgname")'.
  
  
  Attaching package: 'Biobase'
  
  The following object is masked from 'package:MatrixGenerics':
  
      rowMedians
  
  The following objects are masked from 'package:matrixStats':
  
      anyMissing, rowMedians
  
  
  Attaching package: 'stageR'
  
  The following object is masked from 'package:methods':
  
      getMethod
  
  Error in `[<-`(`*tmp*`, idCon, 1, value = unlist(txLevelAdjustments)) : 
    subscript out of bounds
  Calls: stageWiseAdjustment -> stageWiseAdjustment -> .local -> .stageWiseTest
  Execution halted

Relevant files

[nextflow.log](https://github.com/nf-core/rnasplice
splicing_P107513878.log
/files/12173874/nextflow.log)

System information

nextflow/23.04.1
debian 10
slurm
dev version

GTF_2_GFF3 fails with latest Gencode GTF for human

Description of the bug

The pipeline fails when running with --rmats and the latest GTF file for human for Gencode: https://ftp.ebi.ac.uk/pub/databases/gencode/Gencode_human/release_43/gencode.v43.annotation.gtf.gz, even though --gencode is specified in the command.

GTF file source: https://www.gencodegenes.org/human/

I'm including a command below that reproduces the error. The sample sheet and contrast sheet are based on the pipeline's test profile, but I've customized the GTF and reference genome.

Command used and terminal output

nextflow run nf-core/rnasplice -r dev -latest -profile docker --outdir test-small-rnasplice --gencode --genome GRCh38 \
--input https://raw.githubusercontent.com/nf-core/test-datasets/rnasplice/samplesheet/samplesheet.csv \
--contrasts https://raw.githubusercontent.com/nf-core/test-datasets/rnasplice/samplesheet/contrastsheet.csv \
--gtf https://ftp.ebi.ac.uk/pub/databases/gencode/Gencode_human/release_43/gencode.v43.annotation.gtf.gz --rmats --rmats_read_len 75 --rmats_paired_stats --aligner star_salmon --dexseq_exon


ERROR ~ Error executing process > 'NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3'

Caused by:
  Process `NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3` terminated with an error exit status (139)

Command executed:

  gffread gencode.v43.annotation.gtf -L | awk -F'	' -vOFS='	' '{ gsub("transcript", "mRNA", $3); print}' > gencode.v43.annotation_genes.gff3
  
  cat <<-END_VERSIONS > versions.yml
  "NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:GTF_2_GFF3":
      gffread: $(gffread --version 2>&1)
  END_VERSIONS

Command exit status:
  139

Command output:
  (empty)

Command error:
  .command.sh: line 2:    28 Segmentation fault      (core dumped) gffread gencode.v43.annotation.gtf -L
          30 Done                    | awk -F'	' -vOFS='	' '{ gsub("transcript", "mRNA", $3); print}' > gencode.v43.annotation_genes.gff3

Relevant files

No response

System information

No response

EDGER_EXON fails if only single entry in contrast sheet

Description of the bug

My contrast sheet looks like this:

contrast,treatment,control
KO_CONTROL,KO,CONTROL

then I get

  Loading required package: limma
  Error in asplit(contrasts, MARGIN = 2) : 
    dim(x) must have a positive length

however, making a new fake contrast sheet with also the reverse contrast fixes it.

contrast,treatment,control
KO_CONTROL,KO,CONTROL
CONTROL_KO,CONTROL,KO

The exact place the error occurs is in the script run_edger_exon.R

DGELRT.exprs <- mapply(
    FUN      = glmQLFTest,
    contrast = asplit(contrasts, MARGIN = 2),
    MoreArgs = list(glmfit = DGEGLM),
    SIMPLIFY = FALSE
)

Command used and terminal output

nextflow run \
	/omics/groups/xxxxx/internal/xxxxx/src/github.com/dkoppstein/rnasplice \
	--input config/samplesheet_splicing.csv \
	--contrasts config/contrastsheet_splicing.csv \
	--outdir workspace/rnasplice_results_ko_vs_control \
	-c config/dkfz.config \
	--fasta $(GENOMEDIR)/GRCh38.primary_assembly.genome.fa \
	--gtf $(GENOMEDIR)/gencode.v43.annotation.gtf \
	--star_index $(GENOMEDIR)/genome/index/star \
	--salmon_index $(GENOMEDIR)/genome/index/salmon \
	--gencode \
	--save_reference \
	--min_samps_gene_expr 0 \
	--min_samps_feature_expr 0 \
	--min_samps_feature_prop 0 \
	--min_feature_expr 0 \
	--min_feature_prop 0 \
	--min_gene_expr 0 \
	--miso_genes "ENSG00000004961.15, ENSG00000005302.19, ENSG00000147403.18" \
	-resume
	touch $@

Relevant files

No response

System information

Nextflow version 23.04.1 build 5866
HPC
lsf executor
Singularity container
CentOS Linux
dev

SUPPA cluster events error

Description of the bug

Hi,
I am trying dev version and I encountered the following error:

I have 32 samples total, 4 conditions, 8 samples per condition

Best


Error executing process > 'NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:CLUSTEREVENTS_IOE (CP-Cortex)

Caused by:
  Process `NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:CLUSTEREVENTS_IOE (CP-Cortex)` terminated with an error exit status (1)

Command executed:

  suppa.py \
      clusterEvents \
      --dpsi CP-Cortex_local_diffsplice.dpsi \
      --psivec CP-Cortex_local_diffsplice.psivec \
      --dpsi-threshold 0.05 \
      --eps 0.05 \
      --metric euclidean \
      --min-pts 20 \
      --groups 1-25,6-27,12-30,17-32 \
      --clustering DBSCAN \
        -o CP-Cortex_local_cluster
  
  cat <<-END_VERSIONS > versions.yml
  "NFCORE_RNASPLICE:RNASPLICE:SUPPA_SALMON:CLUSTEREVENTS_IOE":
      suppa: $(python -c "import pkg_resources; print(pkg_resources.get_distribution('suppa').version)")
  END_VERSIONS

Command exit status:
  1

Command output:
  (empty)

Command error:
  ERROR:lib.cluster_tools:Invalid index. Index 32 is larger than the number of columns in the file (16).`


Command used and terminal output

nextflow run nf-core/rnasplice --input $wd/samplesheet.csv \
							   --contrasts $wd/contrast.csv \
							   --outdir splice_attempt1 \
							   --genome GRCm38 \
							   --aligner star_salmon \
							   --min_samps_gene_expr 2 \
							   --min_samps_feature_expr 2 \
							   --min_gene_expr 5 \
							   --min_feature_expr 5 \
							   --min_feature_prop 0.2 \
							   --dexseq_exon true \
							   --edger_exon true\
							   --dexseq_dtu true \
							   --dtu_txi scaledTPM \
							   --rmats true \
							   --rmats_read_len 75 \
							   --suppa true \
							   --suppa_per_isoform true \
							   --save_reference true \
							   --sashimi_plot true \
							   -config config.config \
							   -profile singularity \
							   -r dev

Relevant files

nextflow.log

System information

nextflow/22.10.4
Debian 10
Slurn

EXITING because of FATAL ERROR: Genome version: 20201 is INCOMPATIBLE with running STAR version: 2.7.9a

Description of the bug

Execution cancelled -- Finishing pending tasks before exit
-[nf-core/rnasplice] Pipeline completed with errors-
ERROR ~ Error executing process > 'NFCORE_RNASPLICE:RNASPLICE:ALIGN_STAR:STAR_ALIGN (ERR204916)'

Caused by:
  Process `NFCORE_RNASPLICE:RNASPLICE:ALIGN_STAR:STAR_ALIGN (ERR204916)` terminated with an error exit status (105)

Command executed:

  STAR \
      --genomeDir STARIndex \
      --readFilesIn input1/ERR204916_1_val_1.fq.gz input2/ERR204916_2_val_2.fq.gz \
      --runThreadN 12 \
      --outFileNamePrefix ERR204916. \
       \
      --sjdbGTFfile genes_chrX.gtf \
      --outSAMattrRGline 'ID:ERR204916'  'SM:ERR204916'  \
      --quantMode TranscriptomeSAM --twopassMode Basic --outSAMtype BAM Unsorted --readFilesCommand gunzip -c --runRNGseed 0 --outFilterMultimapNmax 20 --alignSJDBoverhangMin 1 --outSAMattributes NH HI AS NM MD--quantTranscriptomeBan Singleend



  if [ -f ERR204916.Unmapped.out.mate1 ]; then
      mv ERR204916.Unmapped.out.mate1 ERR204916.unmapped_1.fastq
      gzip ERR204916.unmapped_1.fastq
  fi
  if [ -f ERR204916.Unmapped.out.mate2 ]; then
      mv ERR204916.Unmapped.out.mate2 ERR204916.unmapped_2.fastq
      gzip ERR204916.unmapped_2.fastq
  fi

  cat <<-END_VERSIONS > versions.yml
  "NFCORE_RNASPLICE:RNASPLICE:ALIGN_STAR:STAR_ALIGN":
      star: $(STAR --version | sed -e "s/STAR_//g")
      samtools: $(echo $(samtools --version 2>&1) | sed 's/^.*samtools //; s/Using.*$//')
      gawk: $(echo $(gawk --version 2>&1) | sed 's/^.*GNU Awk //; s/, .*$//')
  END_VERSIONS

Command exit status:
  105

Command output:
  	STAR --genomeDir STARIndex --readFilesIn input1/ERR204916_1_val_1.fq.gz input2/ERR204916_2_val_2.fq.gz --runThreadN 12 --outFileNamePrefix ERR204916. --sjdbGTFfile genes_chrX.gtf --outSAMattrRGline ID:ERR204916 SM:ERR204916 --quantMode TranscriptomeSAM --twopassMode Basic --outSAMtype BAM Unsorted --readFilesCommand gunzip -c --runRNGseed 0 --outFilterMultimapNmax 20 --alignSJDBoverhangMin 1 --outSAMattributesNH HI AS NM MD --quantTranscriptomeBan Singleend
  	STAR version: 2.7.9a   compiled: 2021-05-04T09:43:56-0400 vega:/home/dobin/data/STAR/STARcode/STAR.master/source
  Jan 17 03:25:16 ..... started STAR run
  Jan 17 03:25:16 ..... loading genome

Command error:
  WARNING: Your kernel does not support swap limit capabilities or the cgroup is not mounted. Memory limited without swap.
  	STAR --genomeDir STARIndex --readFilesIn input1/ERR204916_1_val_1.fq.gz input2/ERR204916_2_val_2.fq.gz --runThreadN 12 --outFileNamePrefix ERR204916. --sjdbGTFfile genes_chrX.gtf --outSAMattrRGline ID:ERR204916 SM:ERR204916 --quantMode TranscriptomeSAM --twopassMode Basic --outSAMtype BAM Unsorted --readFilesCommand gunzip -c --runRNGseed 0 --outFilterMultimapNmax 20 --alignSJDBoverhangMin 1 --outSAMattributesNH HI AS NM MD --quantTranscriptomeBan Singleend
  	STAR version: 2.7.9a   compiled: 2021-05-04T09:43:56-0400 vega:/home/dobin/data/STAR/STARcode/STAR.master/source
  Jan 17 03:25:16 ..... started STAR run
  Jan 17 03:25:16 ..... loading genome

  EXITING because of FATAL ERROR: Genome version: 20201 is INCOMPATIBLE with running STAR version: 2.7.9a
  SOLUTION: please re-generate genome from scratch with running version of STAR, or with version: 2.7.4a

  Jan 17 03:25:16 ...... FATAL ERROR, exiting

Work dir:
  /ceph_disk3/mengpf/work/Project/Nextflow/rnasplice/work/5b/2c86f21fb9af7fc6b71f96eac9a670

Tip: you can replicate the issue by changing to the process work dir and entering the command `bash .command.run`

 -- Check '.nextflow.log' file for details

Command used and terminal output

nextflow run rnasplice/main.nf \
--input samplesheet.csv \
--contrasts contrastsheet.csv    \
--genome GRCh37    \
--outdir result \
-profile docker \
--fasta /ceph_disk3/mengpf/work/Project/Nextflow/rnasplice/data/ref/X.fa.gz \
--gtf /ceph_disk3/mengpf/work/Project/Nextflow/rnasplice/data/ref/genes_chrX.gtf  \
--star_index /ceph_disk3/mengpf/work/Project/Nextflow/rnasplice/data/ref/STARIndex/

Relevant files

No response

System information

No response

sashimi_plot error

Description of the bug

I'm getting an error message when running rnasplice about the sashimi_plot. The error message is copied below:

-[nf-core/rnasplice] Pipeline completed with errors-
ERROR ~ Error executing process > 'NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI (3)'

Caused by:
Process NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI (3) terminated with an error exit status (1)

Command executed:

sashimi_plot --plot-event ENSG00000147403 index miso_settings.txt --output-dir sashimi

cat <<-END_VERSIONS > versions.yml
"NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI":
python: $(python --version | sed "s/Python //g")
misopy: $(python -c "import pkg_resources; print(pkg_resources.get_distribution('misopy').version)")
END_VERSIONS

Command exit status:
1

Command output:
(empty)

Command error:
/usr/local/lib/python2.7/site-packages/matplotlib/cbook/deprecation.py:107: MatplotlibDeprecationWarning: The mpl_toolkits.axes_grid module was deprecated in version 2.1. Use mpl_toolkits.axes_grid1 and mpl_toolkits.axisartist provies the same functionality instead.
warnings.warn(message, mplDeprecation, stacklevel=1)
Traceback (most recent call last):
File "/usr/local/bin/sashimi_plot", line 11, in
sys.exit(main())
File "/usr/local/lib/python2.7/site-packages/misopy/sashimi_plot/sashimi_plot.py", line 276, in main
plot_label=plot_label)
File "/usr/local/lib/python2.7/site-packages/misopy/sashimi_plot/sashimi_plot.py", line 142, in plot_event
%(event_name, pickle_dir)
Exception: Event ENSG00000147403 not found in pickled directory index. Are you sure this is the right directory for the event?

Command used and terminal output

This is the command I ran:
nextflow run nf-core/rnasplice -profile docker -params-file params.yaml

This was my params.yaml file:
input: '/path/samplesheet.csv'
contrasts: '/path/contrastsheet.csv'
outdir: '/path/outdir/'
source: 'fastq'
genome: 'BDGP6'
aligner: 'star_salmon'
save_reference: true
dexseq_dtu: true
min_samps_gene_expr: 6
min_gene_expr: 10
min_samps_feature_expr: 3
min_feature_expr: 10
min_samps_feature_prop: 3
min_feature_prop: 0.1

This was my Contrastsheet:
contrast,treatment,control
AUB_CS,AUB,CS

Relevant files

No response

System information

Nextflow version: version 23.10.0
Linux OS
Version of nf-core/rnasplice 1.0.1

MISO_SASHIMI looks in NXF_HOME subdirectory instead of working directory for output files

Description of the bug

Here, $NXF_HOME is set to /omics/groups/xxxxx/internal/xxxxx/.nextflow.

miso_prefix gets set to miso_prefix: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data. Therefore, it looks for the output file /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188383_sorted which doesn't exist, but the actual location should be in the working directory test_local. Actually, the _sorted directories are not created there.

(base) -bash-4.2$ ls test_local/misopy/miso_data/
ERR188383  ERR188428  ERR188454  ERR204916

Complete error:

 -[nf-core/rnasplice] Pipeline completed with errors-
ERROR ~ Error executing process > 'NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI (1)'

Caused by:
  Process `NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI (1)` terminated with an error exit status (1)

Command executed:

  sashimi_plot --plot-event ENSG00000004961 index miso_settings.txt --output-dir sashimi
 
  cat <<-END_VERSIONS > versions.yml
  "NFCORE_RNASPLICE:RNASPLICE:VISUALISE_MISO:MISO_SASHIMI":
      python: $(python --version | sed "s/Python //g")
      misopy: $(python -c "import pkg_resources; print(pkg_resources.get_distribution('misopy').version)")
  END_VERSIONS

Command exit status:
  1

Command output:
  Reading settings from: miso_settings.txt
  Parsing data:bam_prefix
  Parsing data:miso_prefix
  Parsing data:bam_files
  Parsing data:miso_files
  Parsing plotting:fig_width
  Parsing plotting:fig_height
  Parsing plotting:intron_scale
  Parsing plotting:exon_scale
  Parsing plotting:logged
  Parsing plotting:font_size
  Parsing plotting:ymax
  Parsing plotting:show_posteriors
  Parsing plotting:bar_posteriors
  Parsing plotting:number_junctions
  Parsing plotting:resolution
  Parsing plotting:posterior_bins
  Parsing plotting:gene_posterior_ratio
  Parsing plotting:colors
  Parsing plotting:bar_color
  Parsing plotting:bf_thresholds
  miso_prefix: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data
  Searching for MISO files in: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188383_sorted
    - Looking for chromosome X directories
  Error: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188383_sorted not a directory.
  Error: Could not find MISO output files for sample ERR188383_sorted (after searching in /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188383_sorted and its subdirectories). Are you sure MISO output files are present in that directory?
  Searching for MISO files in: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188428_sorted
    - Looking for chromosome X directories
  Error: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188428_sorted not a directory.
  Error: Could not find MISO output files for sample ERR188428_sorted (after searching in /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188428_sorted and its subdirectories). Are you sure MISO output files are present in that directory?
  Searching for MISO files in: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188454_sorted
    - Looking for chromosome X directories
  Error: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188454_sorted not a directory.
  Error: Could not find MISO output files for sample ERR188454_sorted (after searching in /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188454_sorted and its subdirectories). Are you sure MISO output files are present in that directory?
  Searching for MISO files in: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR204916_sorted
    - Looking for chromosome X directories
  Error: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR204916_sorted not a directory.
  Error: Could not find MISO output files for sample ERR204916_sorted (after searching in /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR204916_sorted and its subdirectories). Are you sure MISO output files are present in that directory?
  Reading dimensions from settings...
   - Height: 7.00
   - Width: 7.00
  Plotting read densities and MISO estimates along event...
    - Event: ENSG00000004961
  Setting up plot using dimensions:  [7.0, 7.0]
  Using intron scale  30.0
  Using exon scale  4.0
  Reading sample label: ERR188383_sorted.bam
  Processing BAM: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/star/ERR188383_sorted.bam

Command error:
  Parsing plotting:number_junctions
  Parsing plotting:resolution
  Parsing plotting:posterior_bins
  Parsing plotting:gene_posterior_ratio
  Parsing plotting:colors
  Parsing plotting:bar_color
  Parsing plotting:bf_thresholds
  miso_prefix: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data
  Searching for MISO files in: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188383_sorted
    - Looking for chromosome X directories
  Error: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188383_sorted not a directory.
  Error: Could not find MISO output files for sample ERR188383_sorted (after searching in /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188383_sorted and its subdirectories). Are you sure MISO output files are present in that directory?
  Searching for MISO files in: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188428_sorted
    - Looking for chromosome X directories
  Error: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188428_sorted not a directory.
  Error: Could not find MISO output files for sample ERR188428_sorted (after searching in /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188428_sorted and its subdirectories). Are you sure MISO output files are present in that directory?
  Searching for MISO files in: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188454_sorted
    - Looking for chromosome X directories
  Error: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188454_sorted not a directory.
  Error: Could not find MISO output files for sample ERR188454_sorted (after searching in /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR188454_sorted and its subdirectories). Are you sure MISO output files are present in that directory?
  Searching for MISO files in: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR204916_sorted
    - Looking for chromosome X directories
  Error: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR204916_sorted not a directory.
  Error: Could not find MISO output files for sample ERR204916_sorted (after searching in /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/misopy/miso_data/ERR204916_sorted and its subdirectories). Are you sure MISO output files are present in that directory?
  Reading dimensions from settings...
   - Height: 7.00
   - Width: 7.00
  Plotting read densities and MISO estimates along event...
    - Event: ENSG00000004961
  Setting up plot using dimensions:  [7.0, 7.0]
  Using intron scale  30.0
  Using exon scale  4.0
  Reading sample label: ERR188383_sorted.bam
  Processing BAM: /omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/star/ERR188383_sorted.bam
  Traceback (most recent call last):
    File "/usr/local/bin/sashimi_plot", line 11, in <module>
      sys.exit(main())
    File "/usr/local/lib/python2.7/site-packages/misopy/sashimi_plot/sashimi_plot.py", line 276, in main
      plot_label=plot_label)
    File "/usr/local/lib/python2.7/site-packages/misopy/sashimi_plot/sashimi_plot.py", line 153, in plot_event
      plot_label=plot_label)
    File "/usr/local/lib/python2.7/site-packages/misopy/sashimi_plot/plot_utils/plot_gene.py", line 698, in plot_density_from_file
      plot_title=plot_title)
    File "/usr/local/lib/python2.7/site-packages/misopy/sashimi_plot/plot_utils/plot_gene.py", line 260, in plot_density
      junction_log_base=junction_log_base)
    File "/usr/local/lib/python2.7/site-packages/misopy/sashimi_plot/plot_utils/plot_gene.py", line 48, in plot_density_single
      bamfile = pysam.Samfile(bam_filename, 'rb')
    File "pysam/libcalignmentfile.pyx", line 751, in pysam.libcalignmentfile.AlignmentFile.__cinit__
    File "pysam/libcalignmentfile.pyx", line 950, in pysam.libcalignmentfile.AlignmentFile._open
  IOError: [Errno 2] could not open alignment file `/omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/test_local/star/ERR188383_sorted.bam`: No such file or directory

Work dir:
  /omics/odcf/analysis/xxxxx_projects/sb_tall_lines/nextflow/work/99/c923adb950181d6c7810fcdf94cecc

Tip: view the complete command output by changing to the process work dir and entering the command `cat .command.out`

 -- Check '.nextflow.log' file for details


Command used and terminal output

nextflow run nf-core/rnasplice -profile test -c local.config --outdir test_local -r dev

Relevant files

local.config

params {
    config_profile_description = 'Deutsches Krebsforschungszentrum (DKFZ) HPC cluster profile provided by nf-core/configs'
    config_profile_contact     = 'Kübra Narcı [email protected]'
    config_profile_name        = 'DKFZ cluster'


    max_cpus   = 16
    max_memory = '48.GB'
    max_time   = '48.h'
}


singularity {
  enabled = true
  autoMounts = true
}

process {
  executor = 'local'
}

executor {
  name = 'local'
  cpus = 16
  memory = '48 GB'
}

System information

  • Nextflow version: 23.04.1 build 5866
  • Hardware: LSF HPC
  • Executor: 'local'
  • Container engine: Singularity
  • OS: CentOS 7 Linux
  • Version of nf-core/rnasplice: dev

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