CRISPR-based targeted haplotype-resolved assembly of a megabase region

被引:6
|
作者
Li, Taotao [1 ,2 ,3 ]
Du, Duo [1 ,2 ,3 ]
Zhang, Dandan [1 ,2 ,3 ]
Lin, Yicheng [1 ,2 ,3 ]
Ma, Jiakang [1 ,2 ,3 ]
Zhou, Mengyu [1 ,2 ,3 ]
Meng, Weida [1 ,2 ,3 ]
Jin, Zelin [1 ,2 ,3 ]
Chen, Ziqiang [1 ,2 ,3 ]
Yuan, Haozhe [1 ,2 ,3 ]
Wang, Jue [1 ,2 ,3 ]
Dong, Shulong [1 ,2 ,3 ]
Sun, Shaoyang [4 ]
Ye, Wenjing [5 ]
Li, Bosen [4 ]
Liu, Houbao [6 ]
Zhang, Zhao [4 ]
Jiao, Yuchen [7 ]
Xie, Zhi [8 ]
Qiu, Wenqing [1 ,3 ,9 ]
Liu, Yun [1 ,2 ,3 ]
机构
[1] Fudan Univ, Shanghai Xuhui Cent Hosp, Sch Basic Med Sci, Dept Biochem & Mol Biol,MOE Key Lab Metab & Mol Me, Shanghai, Peoples R China
[2] Fudan Univ, Inst Brain Sci, State Key Lab Med Neurobiol, Shanghai, Peoples R China
[3] Fudan Univ, Inst Brain Sci, MOE Frontiers Ctr Brain Sci, State Key Lab Med Neurobiol, Shanghai, Peoples R China
[4] Fudan Univ, Sch Basic Med Sci, Dept Biochem & Mol Biol, MOE Key Lab Metab & Mol Med, Shanghai, Peoples R China
[5] Fudan Univ, Huashan Hosp, Div Rheumatol & Immunol, Shanghai, Peoples R China
[6] Fudan Univ, Zhongshan Hosp, Dept Gen Surg, Shanghai, Peoples R China
[7] Chinese Acad Med Sci & Peking Union Med Coll, Canc Hosp, Natl Canc Ctr, Natl Clin Res Ctr Canc,State Key Lab Mol Oncol, Beijing, Peoples R China
[8] Sun Yat Sen Univ, Zhongshan Ophthalm Ctr, State Key Lab Ophthalmol, Guangzhou, Peoples R China
[9] Fudan Univ, Human Phenome Inst, Zhangjiang Fudan Int Innovat Ctr, Shanghai, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
DNA METHYLATION; GENOME; ALIGNMENT; GENES;
D O I
10.1038/s41467-022-35389-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Constructing high-quality haplotype-resolved genome assemblies has substantially improved the ability to detect and characterize genetic variants. A targeted approach providing readily access to the rich information from haplotype-resolved genome assemblies will be appealing to groups of basic researchers and medical scientists focused on specific genomic regions. Here, using the 4.5 megabase, notoriously difficult-to-assemble major histocompatibility complex (MHC) region as an example, we demonstrated an approach to construct haplotype-resolved assembly of the targeted genomic region with the CRISPR-based enrichment. Compared to the results from haplotype-resolved genome assembly, our targeted approach achieved comparable completeness and accuracy with reduced computing complexity, sequencing cost, as well as the amount of starting materials. Moreover, using the targeted assembled personal MHC haplotypes as the reference both improves the quantification accuracy for sequencing data and enables allele-specific functional genomics analyses of the MHC region. Given its highly efficient use of resources, our approach can greatly facilitate population genetic studies of targeted regions, and may pave a new way to elucidate the molecular mechanisms in disease etiology. Low-cost targeted approach to construct haplotype-resolved assemblies is needed to facilitate population genetic studies. Here, the authors demonstrate assembling high-quality MHC haplotypes with CRISPR-based enrichment and long-read sequencings.
引用
收藏
页数:15
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