The proportion of pathogenic rare nsSNVs and total load of pathogenic derived alleles in 8 HapMap subjects with high coverage sequencing data.
收藏Figshare2015-12-02 更新2026-04-29 收录
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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.
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2015-12-02



