Hi
I have NGS data for several whole genome sequences and I want to determine the accuracy of base calling by comparing the variants with those present in Illumina OmniExpress BeadChip Array for the same samples in a GWAS dataset generated using iScan.
Has anyone worked on this?
Thanks in advance
I have NGS data for several whole genome sequences and I want to determine the accuracy of base calling by comparing the variants with those present in Illumina OmniExpress BeadChip Array for the same samples in a GWAS dataset generated using iScan.
Has anyone worked on this?
Thanks in advance