The proportion of pathogenic rare nsSNVs and total load of pathogenic derived alleles in 8 HapMap subjects with high coverage sequencing data.
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aThe nsSNVs with missing scores at SIFT and/or MutationTaster were not used in the estimation. bthe 95% confidence interval was derived empirically from randomly repeating 10-fold cross-validation 200 times.
创建时间：
2013-01-17
