Additional file 4: of Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genes
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https://springernature.figshare.com/articles/Additional_file_4_of_Whole_exome_sequencing_in_adult-onset_hearing_loss_reveals_a_high_load_of_predicted_pathogenic_variants_in_known_deafness-associated_genes_and_identifies_new_candidate_genes/7047242/1
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Table S1. which lists the software prediction tools used to call and annotate variants, with relevant references. (XLS 30 kb)
创建时间：
2018-09-05
