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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https://figshare.com/articles/dataset/_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_/176270
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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
