Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
410
stars
418
forks
source link
Samplesheets with more normal-samples per patient pass nf-validation #1293
Open
asp8200 opened 1 year ago
Description of the bug
Samplesheets with more normal-samples per patient pass nf-validation, but they (probably) shouldn't.
https://nfcore.slack.com/archives/CGFUX04HZ/p1698056996871649?thread_ts=1697539431.495609&cid=CGFUX04HZ
The issue can be reproduced by using this csv:
which is just
tests/csv/3.0/recalibrated_somatic_joint.csv
wheresample2
has changed status from0
(normal) to1
(tumor).@FriederikeHanssen knows what this is about ;-)
Command used and terminal output
Relevant files
No response
System information
No response