Abstract
Genetic maps are fundamental resources for linkage and association studies. A fine-scale genetic map can be constructed by inferring historical recombination events from the genome-wide structure of linkage disequilibrium—a non-random association of alleles among loci—by using population-scale sequencing data. We constructed a fine-scale genetic map and identified recombination hotspots from 10,092,573 bi-allelic high-quality autosomal markers segregating among 150 unrelated Japanese individuals. These individuals’ genotypes were determined by high-coverage (30×) whole-genome sequencing, and the genotype quality was carefully controlled by using their parents’ and offspring’s genotypes. The pedigree information was also utilized for haplotype phasing. The resulting genome-wide recombination rate profiles were concordant with those of the HapMap worldwide population on a broad scale, and the resolution was much improved. We identified 9487 recombination hotspots and confirmed the enrichment of previously known motifs in the hotspots. Moreover, we demonstrated that the Japanese genetic map improved the haplotype phasing and genotype imputation accuracy for the Japanese population. The construction of a population-specific genetic map will help make genetics research more accurate.
Competing Interest Statement
The authors have declared no competing interest.
Footnotes
Conflict of Interest: The authors declare no conflict of interest.
