Use of whole‐genome variants and their frequency data to estimate haplotype structure in the Thoroughbred genome.

Use of whole-genome variants and their frequency data to estimate haplotype structure in the Thoroughbred genome In our previous study, whole-genome sequencing of 101 Thoroughbred horses was performed, and the allele frequencies of the detected single nucleotide variants (SNVs) were made available (Tozaki et al., [3]). If SNVs identified by genome-wide association studies were located far from true SNVs, it was considered possible to search for truly causative variants by estimating haplotype structure using our genome-wide variant database. [Extracted from the article]

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