Assembly and analysis of 100 full MHC haplotypes from the Danish population

被引:14
|
作者
Jensen, Jacob M. [1 ]
Villesen, Palle [1 ,2 ]
Friborg, Rune M. [1 ]
Mailund, Thomas [1 ]
Besenbacher, Soren [1 ,3 ]
Schierup, Mikkel H. [1 ,4 ]
机构
[1] Aarhus Univ, Bioinformat Res Ctr, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ, Dept Clin Med, DK-8200 Aarhus N, Denmark
[3] Aarhus Univ Hosp, Dept Mol Med, DK-8200 Aarhus N, Denmark
[4] Aarhus Univ, Dept Biosci, DK-8000 Aarhus C, Denmark
关键词
STRUCTURAL VARIATION; ALIGNMENT; SEQUENCE; RECOMBINATION; PERFORMANCE; ANNOTATION; EVOLUTION; GENOMES; DENMARK; REGION;
D O I
10.1101/gr.218891.116
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Genes in the major histocompatibility complex (MHC, also known as HLA) play a critical role in the immune response and variation within the extended 4-Mb region shows association with major risks of many diseases. Yet, deciphering the underlying causes of these associations is difficult because the MHC is the most polymorphic region of the genome with a complex linkage disequilibrium structure. Here, we reconstruct full MHC haplotypes from de novo assembled trios without relying on a reference genome and perform evolutionary analyses. We report 100 full MHC haplotypes and call a large set of structural variants in the regions for future use in imputation with GWAS data. We also present the first complete analysis of the recombination landscape in the entire region and show how balancing selection at classical genes have linked effects on the frequency of variants throughout the region.
引用
收藏
页码:1597 / 1607
页数:11
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