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.
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Univ Massachusetts, Biomed Engn & Biotechnol Program, Lowell, MA 01854 USA
Massachusetts Bay Community Coll, Biotechnol & Forens DNA Sci Program, Wellesley Hills, MA 02481 USAUniv Massachusetts, Biomed Engn & Biotechnol Program, Lowell, MA 01854 USA
Wilson, Jamie L.
Saint-Louis, Vertus
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Univ Haiti, Ecole Normale Super, Port Au Prince, HaitiUniv Massachusetts, Biomed Engn & Biotechnol Program, Lowell, MA 01854 USA
Saint-Louis, Vertus
Auguste, Jensen O.
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Massachusetts Bay Community Coll, Biotechnol & Forens DNA Sci Program, Wellesley Hills, MA 02481 USAUniv Massachusetts, Biomed Engn & Biotechnol Program, Lowell, MA 01854 USA
Auguste, Jensen O.
Jackson, Bruce A.
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Univ Massachusetts, Biomed Engn & Biotechnol Program, Lowell, MA 01854 USA
Massachusetts Bay Community Coll, Biotechnol & Forens DNA Sci Program, Wellesley Hills, MA 02481 USAUniv Massachusetts, Biomed Engn & Biotechnol Program, Lowell, MA 01854 USA