Comments (2)
I did a bit more digging -- running it with NXF_DEBUG=1 reveals that two different temporary directories from two different LSF jobs are being used. Specifically, the error is
Exception: Error: no filename /local/xxxxx/20769714/nxf.98A1VB7d5I/index/chrX/ENSG00000005302.pickle
but the job is being executed in /local/xxxxx/20769804/nxf.YYBkdvf6cO
:
/bin/bash -c cd /local/xxxxx/20769804/nxf.YYBkdvf6cO; eval export PYTHONNOUSERSITE="1" export R_PROFILE_USER="/.Rprofile" export R_ENVIRON_USER="/.Renviron" export JULIA_DEPOT_PATH="/usr/local/share/julia" export PATH="$PATH:/omics/groups/xxxxx/internal/xxxxx/.nextflow/assets/nf-core/rnasplice/bin"; /bin/bash /omics/odcf/analysis/xxxxx/xxxxx/nextflow/work/33/439d4c44670b38d3bd71734475398f/.command.run nxf_trace
I think the specific problem arises because miso somehow hard-encodes the path in the index. Specifically, if I look for the LSF job ID in the index_gff
working directory, I see that
(base) -bash-4.2$ grep -R 20769714 *
Binary file index/genes_to_filenames.shelve.dat matches
so, I suspect that index_gff
is hard-encoding the absolute path to the filename. It might be necessary to explicitly specify scratch false
for this step. I will try this now.
from rnasplice.
In my hands, setting scratch false
in the module seems to make it work (see here). However, is it better to do this in the module, or in conf/modules.config
?
from rnasplice.
Related Issues (17)
- dexseq: stager.R: subscript out of bounds. HOT 2
- prepare_genome gencode HOT 2
- check_contrastsheet not identifying headers even though they're present HOT 2
- DRIMSEQ_FILTER error HOT 10
- ERROR ~ No such variable: Exception evaluating property 'out' for nextflow.script.ChannelOut HOT 7
- SUPPA cluster events error HOT 14
- GTF_2_GFF3 fails with latest Gencode GTF for human HOT 21
- MISO_SASHIMI looks in NXF_HOME subdirectory instead of working directory for output files HOT 4
- The default --miso_genes are invalid when --gencode is specified and cause the pipeline to fail HOT 2
- EDGER_EXON fails if only single entry in contrast sheet HOT 1
- STAGER error: subscript out of bounds HOT 6
- The pipeline should be able to infer strandedness from FASTQ (i.e. allow "auto" for strandedness in the CSV) HOT 2
- Error with rmats.py when running with multiple contrasts: <filename>.bam not found in .rmats files HOT 10
- MISO_SASHIMI error: Could not find MISO output files HOT 4
- test profile: miso_index failure HOT 19
- example contrastsheet.csv missing HOT 1
Recommend Projects
-
React
A declarative, efficient, and flexible JavaScript library for building user interfaces.
-
Vue.js
🖖 Vue.js is a progressive, incrementally-adoptable JavaScript framework for building UI on the web.
-
Typescript
TypeScript is a superset of JavaScript that compiles to clean JavaScript output.
-
TensorFlow
An Open Source Machine Learning Framework for Everyone
-
Django
The Web framework for perfectionists with deadlines.
-
Laravel
A PHP framework for web artisans
-
D3
Bring data to life with SVG, Canvas and HTML. 📊📈🎉
-
Recommend Topics
-
javascript
JavaScript (JS) is a lightweight interpreted programming language with first-class functions.
-
web
Some thing interesting about web. New door for the world.
-
server
A server is a program made to process requests and deliver data to clients.
-
Machine learning
Machine learning is a way of modeling and interpreting data that allows a piece of software to respond intelligently.
-
Visualization
Some thing interesting about visualization, use data art
-
Game
Some thing interesting about game, make everyone happy.
Recommend Org
-
Facebook
We are working to build community through open source technology. NB: members must have two-factor auth.
-
Microsoft
Open source projects and samples from Microsoft.
-
Google
Google ❤️ Open Source for everyone.
-
Alibaba
Alibaba Open Source for everyone
-
D3
Data-Driven Documents codes.
-
Tencent
China tencent open source team.
from rnasplice.