Comments (2)
The issue has been resolved in the dev branch. It occurred because the contrast sheet checker tried to identify the format of your file automatically. Your particular contrast sheet had a lot of "_" characters, so the sniffer thought the file was delimited by this character instead of the "," character. We have now removed the automatic file formatter checker, and require the user to specify the contrast sheet in CSV file format. This is actually what the documentation tells the user to provide, so it is now more-inline with the documentation. Thanks for bringing this to our attention.
Let me know if this has solved your problem and I will close the issue.
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Related Issues (17)
- dexseq: stager.R: subscript out of bounds. HOT 2
- prepare_genome gencode 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 step fails when using scratch directory HOT 2
- 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
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