Additional file 1 of High performance imputation of structural and single nucleotide variants using low-coverage whole genome sequencing
收藏数据链接：
官方服务：
资源简介：
Additional file 1: Table S1.Details of the samples in the reference panel. Table S2. Details of the In-panel samples used in the study. Table S3. Details of the Out-panel samples used in the study. Table S4. Number of SNVs imputed at various PPs and sequencing depths.
提供机构：
figshare创建时间：
2025-03-29
