Comments (4)
Hi,
this issue should be fixed in the development version.
You can give it a try with nextflow run ... -r dev
. If it doesn't work, please let me know!
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Hi @grst I have been able now to test the dev pipeline. Thanks for the update. Unfortunately I am still facing validation issues:
I am using a single end dataset, where there is a fastq_1
, but there is not a fastq_2
.
The input.csv file is similar to:
"sample","fastq_1","fastq_2","strandedness",...
"id1","/path/to/fastq/sample1.fastq.gz","","auto",...
Please note how the fastq_2
column contains empty values.
I'm getting an error validating the 'input' again:
ERROR ~ ERROR: Validation of 'input' file failed!
-- Check '.nextflow.log' file for details
The following errors have been detected:
* -- Entry 1: Missing required value: fastq_2
* -- Entry 2: Missing required value: fastq_2
Having an empty fastq_2
seems correct to me when I check the code at the master
branch. There, if the fastq_2
is empty then the single_end
variable is set to "1"
. You can see this below (specifically line 184, in the not fastq_2
):
scrnaseq/bin/check_samplesheet.py
Lines 181 to 187 in 90cb6a4
However on the dev
branch, the input schema used for the fastq_2
validation must exist and can't be empty:
scrnaseq/assets/schema_input.json
Lines 16 to 30 in 1043441
I'd like for the scrnaseq pipeline to accept an input file with a fastq_2
column filled with ""
(empty strings), since that's what is generated by the nf-core/fetchngs
pipeline when downloading datasets.
Thanks and sorry for the delay in the reply
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Just for further ideas, it may be good to checkout the rnaseq pipeline:
from scrnaseq.
The check is done on purpose. All protocols supported by this pipeline use paired end data, where R1 contains UMI/barcode and R2 the actual sequence.
What kind of single-cell data are you dealing with?
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Related Issues (20)
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