卡纳塔克邦个体基因组计划扩展了人类参考景观,包括南亚。

IF 3.6 Q2 GENETICS & HEREDITY
Apoorva Ganesh, Anisha Mhatre, Yash Chindarkar, Moushmi Goswami, Prakruti Mishra, Aditya Sharma, Manjushri Kalpande, Febina Ravindran, Subhashini Srinivasan, Bibha Choudhary
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引用次数: 0

摘要

组装个体基因组仍然是一项昂贵的努力,阻碍了大规模的比较人类基因组学。迄今为止,仅报道了PR1(波多黎各人)、Ash1(德系犹太人)、Han1(中国南方汉人)和CHM13(北欧人)等少数个体的染色体水平组合。在这里,我们展示了来自印度次大陆(KIn1)的非igsr和非giab个体的染色体水平基因组组装,使用成本效益高的方法获得。我们获得了141 Mb的N50和9的L50,非常接近人类基因组的最大N50和最小L50分别为147 Mb和8。我们还生成了其他印度散居人群的染色体水平组装,包括来自旁遮普、拉合尔的PJL1 (HG03492)、来自古吉拉特邦的GIH1 (NA20847)、来自孟加拉国的BIB1 (HG03009)和来自安得拉邦的ITU1 (HG04217),所有这些都通过构建公开可用的各自的基因组和Hi-C数据在IGSR中表示。在这里,我们通过将这些个体基因组与其他报道的基因组进行比较,证明了在KIn1, Han1, GIH1和BIB1中倒置8p23.1的构型与hg38相似,这里称为8p23.1std。反向构型8p23.1inv存在于CHM13、PJL1、Ash1和PR1中。我们还发现了16号染色体p臂中所有三个已知的大倒位的证据,在南亚人中普遍存在。在第5染色体中,除hg38和Ash1外,所有组合中都存在报道的反转之一。最后,我们研究了KIn1特有的大反转。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Karnataka Individual Genome Project expands the human reference landscape to include South Asia.

Assembling individual genomes remains an expensive endeavor, hindering large-scale comparative human genomics. So far, chromosome-level assemblies of only a few individuals, including PR1 (Puerto Rican), Ash1 (Ashkenazi Jew), Han1 (Southern Han Chinese), and CHM13 (Northern European) have been reported. Here, we present a chromosome-level genome assembly of a non-International Genome Sample Resource (IGSR) and non-Genome in a Bottle individual from the Indian subcontinent (KIn1) obtained using a cost-effective approach. We achieved an N50 of 141 Mb and an L50 of 9-very close to the maximum achievable N50 of 147 Mb and minimum achievable L50 of 8, respectively, for human genomes. We also generated chromosome-level assemblies for other individuals from the Indian diaspora, including PJL1 from Punjab, Lahore (HG03492), GIH1 from Gujarat (NA20847), BIB1 from Bangladesh (HG03009), and ITU1 from Andhra Pradesh (HG04217), all represented in IGSR, by scaffolding the publicly available respective contigs and Hi-C data. Here, we demonstrate that by comparing these individual genomes with those reported elsewhere, the configuration of inversion 8p23.1 in KIn1, Han1, GIH1, and BIB1 is similar to that in hg38, here to referred as 8p23.1std. The inverted configuration, 8p23.1inv, is present in CHM13, PJL1, Ash1, and PR1. We also find evidence of all three large known inversions in the p-arm of chromosome 16, with prevalence among South Asians. In chromosome 5, one of the reported inversions is present in all assemblies except hg38 and Ash1. Finally, we investigate the large inversions that are unique to KIn1.

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来源期刊
HGG Advances
HGG Advances Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
4.30
自引率
4.50%
发文量
69
审稿时长
14 weeks
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