Hi, I have one bam/barcode file per donor (cell line), and I want to get SNPs from each donor, to then be able to identify the donors in a bam/barcode file where they where multiplexed. Does it make sense to run cellsnp-lite per each donor to identify their SNPs, then merge their vcf files for vireo?
Hi, I have one bam/barcode file per donor (cell line), and I want to get SNPs from each donor, to then be able to identify the donors in a bam/barcode file where they where multiplexed. Does it make sense to run cellsnp-lite per each donor to identify their SNPs, then merge their vcf files for vireo?