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Hello
I need a suggestion on running the structural variant calling on hifi data from two SMRT cells. I have two aligned bam files from same subject (run in 2 smart cells, PacBio). I tried doing the variant call for aligned file from each SMRT cell. Then sorted the vcf from each smrt cell but creating index for the vcf fails. Can you suggest a way to run aligned files from different smrt cells and create a single vcf file
Thank you