Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies
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Schematic of germline imputation from low-coverage sequencing. a The
Genome-wide association studies and epigenome-wide association studies go together in cancer control
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Genome-wide generation and genotyping of informative SNPs to scan molecular signatures for seed yield in chickpea
Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies
Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies
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Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores, Genome Medicine
Neogen® SkimSEEK™: Human Low-pass Whole Genome Sequencing and Imputation
An integrated map of genetic variation from 1,092 human genomes
Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies
BIOCELL, Free Full-Text
Frontiers Comparison of Genotype Imputation for SNP Array and Low-Coverage Whole-Genome Sequencing Data