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