A fine-scale genetic map of the Japanese population

IF 2.9 3区 医学 Q2 GENETICS & HEREDITY
Jun Takayama, Satoshi Makino, Takamitsu Funayama, Masao Ueki, Akira Narita, Keiko Murakami, Masatsugu Orui, Mami Ishikuro, Taku Obara, the Tohoku Medical Megabank Project Study Group, Shinichi Kuriyama, Masayuki Yamamoto, Gen Tamiya
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引用次数: 0

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 10 092 551 bi-allelic high-quality autosomal markers segregating among 150 unrelated Japanese individuals whose 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 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.

Abstract Image

日本人口的精细遗传图谱。
基因图谱是进行连锁和关联研究的基础资源。利用种群规模的测序数据,从全基因组的连锁不平衡结构--等位基因在位点间的非随机关联--推断历史重组事件,可以构建精细规模的遗传图谱。我们从 150 个无血缘关系的日本个体中分离出的 10 092 551 个双等位基因高质量常染色体标记中构建了精细的遗传图谱,并确定了重组热点,这些个体的基因型是通过高覆盖率(30×)全基因组测序确定的,并通过使用其父母和后代的基因型对基因型质量进行了严格控制。血统信息也用于单倍型分期。由此得出的全基因组重组率曲线与全球人口的重组率曲线大体一致,分辨率也大大提高。我们发现了 9487 个重组热点,并证实了这些热点中富含以前已知的图案。此外,我们还证明日本基因图谱提高了日本人群的单倍型分期和基因型归因的准确性。构建特定人群的遗传图谱将有助于提高遗传学研究的准确性。
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来源期刊
Clinical Genetics
Clinical Genetics 医学-遗传学
CiteScore
6.50
自引率
0.00%
发文量
175
审稿时长
3-8 weeks
期刊介绍: Clinical Genetics links research to the clinic, translating advances in our understanding of the molecular basis of genetic disease for the practising clinical geneticist. The journal publishes high quality research papers, short reports, reviews and mini-reviews that connect medical genetics research with clinical practice. Topics of particular interest are: • Linking genetic variations to disease • Genome rearrangements and disease • Epigenetics and disease • The translation of genotype to phenotype • Genetics of complex disease • Management/intervention of genetic diseases • Novel therapies for genetic diseases • Developmental biology, as it relates to clinical genetics • Social science research on the psychological and behavioural aspects of living with or being at risk of genetic disease
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