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- Wed Jan 25, 2012 8:10 am
- Forum: Journal Club on Statistical Genomics
- Topic: Imputing newly identified SNPs
- Replies: 3
- Views: 4914
Hello everyone We have used massive parallel sequencing to detect new variants in three genes. We genotyped these new variants + several tag SNPs to completely cover these genes with m.a.f. = 0.1 and r2 = 0.9. After quality control, we had 3216 individuals and 247 SNPs, with a total genotyping rate ...