Additional file 1 of High performance imputation of structural and single nucleotide variants using low-coverage whole genome sequencing
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https://springernature.figshare.com/articles/dataset/Additional_file_1_of_High_performance_imputation_of_structural_and_single_nucleotide_variants_using_low-coverage_whole_genome_sequencing/28689676/1
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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.
提供机构：
Prendergast, James G. D.; Houston, Ross D.; Macqueen, Daniel J.; Robledo, Diego; Gundappa, Manu Kumar; Hamilton, Alastair
创建时间：
2025-03-29
