Efficient phasing and imputation of low-coverage sequencing data

The construction of a haplotype reference panel using extremely

IMPUTE2

Low-coverage sequencing cost-effectively detects known and novel

Imputation of low-coverage sequencing data from 150,119 UK Biobank

Imputation of ancient human genomes

Identifying risk variants for embryo aneuploidy using ultra-low coverage whole-genome sequencing from preimplantation genetic testing - ScienceDirect

Best practices for analyzing imputed genotypes from low-pass

Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an

Cost-effectively dissecting the genetic architecture of complex

Efficient phasing and imputation of low-coverage sequencing data

PDF) NOISYmputer: genotype imputation in bi-parental populations

Sequencing Coverage for NGS Experiments

Evaluating coverage bias in next-generation sequencing of Escherichia coli

Replacement Spreader Rollers by Rooftop Equipment

Detecting selection in low-coverage high-throughput sequencing

Actuarial analysis: Coverage Ratio: The Actuarial Perspective