Efficient phasing and imputation of low-coverage sequencing data
By A Mystery Man Writer
Description
PDF) A cautionary tale of low-pass sequencing and imputation with
Low-coverage whole genome sequencing for a highly selective cohort
Frontiers Comparison of Genotype Imputation for SNP Array and
Frontiers Comparison of Genotype Imputation for SNP Array and
Application of long-read sequencing to the detection of structural variants in human cancer genomes - Computational and Structural Biotechnology Journal
Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an
Assessment of the performance of different imputation methods for
PDF] GeneImp: Fast Imputation to Large Reference Panels Using
Efficient phasing and imputation of low-coverage sequencing data
A cautionary tale of low-pass sequencing and imputation with respect to haplotype accuracy, Genetics Selection Evolution
Low-coverage sequencing cost-effectively detects known and novel
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per adult (price varies by group size)