Efficient phasing and imputation of low-coverage sequencing data using large reference panels

Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies

Best practices for analyzing imputed genotypes from low-pass

Efficient phasing and imputation of low-coverage sequencing data using large reference panels

Frontiers Comparison of Genotype Imputation for SNP Array and

Low-coverage sequencing cost-effectively detects known and novel

Accurate rare variant phasing of whole-genome and whole-exome

A cautionary tale of low-pass sequencing and imputation with respect to haplotype accuracy, Genetics Selection Evolution

Number of SNPs revealed by different imputation methods for different

PDF) Efficient phasing and imputation of low-coverage sequencing data using large reference panels

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