Assessing Reproducibility of Germline Variants Detected with Short-read Whole Genome Sequencing
收藏NIAID Data Ecosystem2026-03-12 收录
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Reproducible germline variant detection with whole genome sequencing (WGS) is vital for the implementation of precision medicine and is a complicated process in which each step affects variant call quality. To dissect the impacts of related factors, we sequenced triplicates of three DNA samples by three short-read sequencing platforms using three library kits in three labs
创建时间：
2021-04-20
