Anyone know a quick way to compare two samples that have undergone exome-sequencing?
I seem to have two samples that have very similar variant call and I wonder if it is actually the same individual. -I have sam and bam files. I have an edited version of the variant call but not the raw vcf files and the moment.
thanks,
Jane
I seem to have two samples that have very similar variant call and I wonder if it is actually the same individual. -I have sam and bam files. I have an edited version of the variant call but not the raw vcf files and the moment.
thanks,
Jane
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