The numbers and proportion of nsSNVs removed by hard-filtering and functional prediction by the logit model in 3 Mendelian-disease patients with in-house exome sequencing data.
收藏Figshare2015-12-02 更新2026-04-29 收录
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aRelated cases with autosomal dominant spinocerebellar ataxia.bCase with neonatal-onset Crohn's disease.cnsSNVs in which prediction is unavailable due to missing scores.
创建时间：
2015-12-02
