Additional file 1 of High performance imputation of structural and single nucleotide variants using low-coverage whole genome sequencing
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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.
创建时间：
2025-03-28
