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To fix, I added a call to vcf-sort in the middle of the POST_PROCESS_VCF script - I tried installing and using bcftools, but it requires a header with the "contig" section which is not present in these intermediate files, and vcftools is already included in the container. Will submit PR for review.
Error from vcftools on process failure is:
Comparing sites in VCF files...
Error: Cannot determine chromosomal ordering of files, both files must contain the same chromosomes to use the diff functions.
Found 10 in file 1 and 1 in file 2.
Looking in the working directory associated with the failing task, POST_PROCESS_VCF produces the file result.DP8.vcf with chromosomes ordered as grep -v "#" result.DP8.vcf | cut -f 1 | uniq | tr "\n" " ":
Possible confounder here is that we are trying to use the Boyle lab's https://github.com/Boyle-Lab/Blacklist for mm10, but using Ensembl build of GRCm38 available from iGenomes - I wrote in a profile into the config as such:
To fix, I added a call to
vcf-sort
in the middle of the POST_PROCESS_VCF script - I tried installing and using bcftools, but it requires a header with the "contig" section which is not present in these intermediate files, and vcftools is already included in the container. Will submit PR for review.Error from vcftools on process failure is:
Looking in the working directory associated with the failing task, POST_PROCESS_VCF produces the file
result.DP8.vcf
with chromosomes ordered asgrep -v "#" result.DP8.vcf | cut -f 1 | uniq | tr "\n" " "
:Possible confounder here is that we are trying to use the Boyle lab's https://github.com/Boyle-Lab/Blacklist for mm10, but using Ensembl build of GRCm38 available from iGenomes - I wrote in a profile into the config as such:
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