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Genomics Proteomics & BioinformaticsGeneticsPeer-reviewed journal article

T2T-YAO: a Telomere-to-telomere Assembled Diploid Reference Genome for Han Chinese

Yukun HeiD, Yanan ChuiD, Shuming GuoiD, Jiang Yong HuiD, Ran LiiD, Yali ZhengiD, Xinqian MaiD, Zhenglin DuiD, Lili ZhaoiD, Wenyi YuiD, Jianbo XueiD, Wenjie BianiD, Feifei YangiD, Xi CheniD, Pingan ZhangiD, Rihan WuiD, Yifan MaiD, Changjun ShaoiD, Jing CheniD, Jian WangiD, Jiwei LiiD, Jing WuiD, Xiaoyi HuiD, Qiuyue LongiD, Mingzheng JiangiD, , Zhancheng GaoiD

PDFDOIPreprint

Abstract

Since its initial release in 2001, the human reference genome has been continuously improved in both continuity and accuracy, and the recently-released telomere-to-telomere version--T2T-CHM13--reaches its top quality after 20 years of effort. However, T2T-CHM13 does not represent an authentic diploid human genome, but rather one derived from a simplified, nearly homozygous genome of a hydatidiform mole cell line. To address this limitation and provide an alternative pertinent to the Chinese population, the largest ethnic group in the world, we have assembled a complete diploid human genome of a male Han Chinese, T2T-YAO, which includes telomere-to-telomere assemblies for all the 22+X+M and 22+Y chromosomes in his two haploids inherited separately from his parents. Both haplotypes contain no artificial sequences or model nucleotides and possess a high quality comparable to CHM13, with fewer than one error per [~]14 Mb. Derived from the individual who lives in the aboriginal region of Han Chinese, T2T-YAO shows clear ancestry and potential genetic continuity from the ancient ancestors of the Han population. Each haplotype of T2T-YAO possesses [~]340 Mb exclusive sequences and [~]3100 unique genes as compared to CHM13, and their genome sequences show greater genetic distance to CHM13 than to each other in terms of nucleotide polymorphism and structural variations. The construction of T2T-YAO would serve as a high-quality diploid reference that enables precise delineation of genomic variations in a haplotype-sensitive manner, which could advance our understandings in human evolution, hereditability of diseases and phenotypes, especially within the context of the unique variations of the Chinese population.

Citations
61
FWCI
5.42
Field percentile
top 2%

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