Comments (3)
I'm also running into the same issue! I thought it was the minimum sample/feature tags, so I set it to zero:
min_samps_gene_expr: 0
min_gene_expr: 0
min_samps_feature_expr: 0
min_feature_expr: 0
min_samps_feature_prop: 0
min_feature_prop: 0
That wasn't the issue either, so I'm hoping someone knows how to solve this.
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Hey @GimenaA
Thanks for reporting your issue. Can you please try with the latest release? I have a feeling you are using an older version where we didn't handle sample names with dashes in them correctly. See this PR for details.
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Closing as completed. Please re-open if you are still facing the same issue.
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Related Issues (20)
- link to example contrastsheet.csv is not working HOT 1
- Empty output for BAM+rMats HOT 2
- make contrasts file names consistent with those of the differentialabundance pipeline HOT 1
- Missing rMATS arguments HOT 2
- DEXSeq-DTU Stager pScreenAdjusted HOT 1
- sashimi_plot error HOT 2
- contrast file problem? HOT 7
- EXITING because of FATAL ERROR: Genome version: 20201 is INCOMPATIBLE with running STAR version: 2.7.9a HOT 2
- MISO error HOT 3
- The processes for splitting files are running very slowly with large numbers of input samples HOT 5
- Error: suppa_split_file.R Input_file must contain samplesheet samples. HOT 2
- ERROR ~ Error executing process > 'NFCORE_RNASPLICE:RNASPLICE:DRIMSEQ_DEXSEQ_DTU_SALMON:DRIMSEQ_FILTER (1)' HOT 11
- Error single-end execution HOT 1
- Error in SUPPA: Clustergroups are assigned incorrectly HOT 4
- test profile: miso_index failure HOT 19
- example contrastsheet.csv missing HOT 1
- Add some more tags to make the pipeline easier to find HOT 1
- DRIMSEQ_FILTER error HOT 5
- STAGER error: subscript out of bounds HOT 4
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