Closed VanessaOak closed 3 years ago
Hello, thanks for your feedback. For now cellSNP would always output chr1-22 & X & Y as contigs into the VCF header (e.g, ##contig=
So besides the VCF header, do the VCF contain any other records of chr20-22? you could check this by
zcat <output.vcf.gz> | grep -v '^#' | awk '{print $1}' | sort -u
which would print all unique chromosomes (the first column) in the VCF.
BTW, could you provide the version of cellSNP (by typing cellSNP
) and the command line you used for your data? Thanks
Thank you for your response. It looks like there are no other records of Chr20-22 so that is good! The version is v0.3.2 Thank you!
That's great. We will fix the issue, making the header of output VCF compatible with the header of input VCF. Thanks!
Hello, I used a VCF file made with the mouse MM10 genome and a 10x BAM file aligned to the mouse MM10 genome. This means my output should have Chromosomes 1-19, M, X, and Y like my input files. But my output from CellSNP contains chromosomes 1-22, X, and Y. Any tips on what I can do to troubleshoot this?