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Efficient phasing and imputation of low-coverage sequencing data using large reference panels
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Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies. - Abstract - Europe PMC
Frontiers Comparison of Genotype Imputation for SNP Array and Low-Coverage Whole-Genome Sequencing Data
A cautionary tale of low-pass sequencing and imputation with respect to haplotype accuracy, Genetics Selection Evolution
A population-specific reference panel for improved genotype imputation in African Americans
Efficient phasing and imputation of low-coverage sequencing data using large reference panels
Accurate rare variant phasing of whole-genome and whole-exome sequencing data in the UK Biobank
PDF) Efficient phasing and imputation of low-coverage sequencing data using large reference panels
SEAD: an augmented reference panel with 22,134 haplotypes boosts the rare variants imputation and GWAS analysis in Asian population
Performance and accuracy evaluation of reference panels for genotype imputation in sub-Saharan African populations - ScienceDirect
PDF] GeneImp: Fast Imputation to Large Reference Panels Using Genotype Likelihoods from Ultralow Coverage Sequencing
A cautionary tale of low-pass sequencing and imputation with respect to haplotype accuracy, Genetics Selection Evolution
PDF] GeneImp: Fast Imputation to Large Reference Panels Using Genotype Likelihoods from Ultralow Coverage Sequencing
