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.
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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：
2013-01-17
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