Konu "Clinical NGS Informatics" için WoS İndeksli Yayınlar Koleksiyonu listeleme
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DEVOUR: Deleterious variants on uncovered regions in whole-exome sequencing
(PeerJ Inc., 2023)The discovery of low-coverage (i.e. uncovered) regions containing clinically significant variants, especially when they are related to the patient's clinical phenotype, is critical for whole-exome sequencing (WES) based ...