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

Frontiers Comparison of Genotype Imputation for SNP Array and Low-Coverage Whole-Genome Sequencing Data

Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations - ScienceDirect

Functional variant analysis across low-coverage and SNP array call

Boosting variant calling performance using a high-quality reference panel for imputing low-coverage sequencing data

PHARP: a pig haplotype reference panel for genotype imputation

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

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Imputation strategies for genomic prediction using nanopore sequencing, BMC Biology

Frontiers Comparison of Genotype Imputation for SNP Array and

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Assessment of the performance of different imputation methods for