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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?
The text was updated successfully, but these errors were encountered:
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?
The text was updated successfully, but these errors were encountered: