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I've identified a potential issue in the recent pipeline release (v2.5.0). It seems the groupTuple command is executed twice during the input channel creation and branching of FASTQ files. As a result, the pipeline is unable to recognise samples processed across multiple lanes, due to an additional layer of file nesting. See here:
I was able to run the pipeline using bismark by adding an underscore "_" inside the name of the sample (in column 1) in the samplesheet.csv
e.g. ( use sample1_rep1 instead of sample1)
Make sure you use 4 header columns instead of 3 being the last genome. (this isn't very clear because the current documentation at https://nf-co.re/methylseq does not mention it! But Felix says it in the conversation
Description of the bug
I've identified a potential issue in the recent pipeline release (v2.5.0). It seems the groupTuple command is executed twice during the input channel creation and branching of FASTQ files. As a result, the pipeline is unable to recognise samples processed across multiple lanes, due to an additional layer of file nesting. See here:
methylseq/workflows/methylseq.nf
Lines 98 to 105 in 66c6138
Command used and terminal output
No response
Relevant files
No response
System information
No response
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