Targeted and complete genomic sequencing of the Major Histocompatibility Complex in haplotypic form of individual heterozygous samples

  1. Dimitri S. Monos3,4
  1. 1 Children's Hospital of Philadelphia;
  2. 2 Delaware Biotechnology Institute, University of Delaware;
  3. 3 Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania
  • * Corresponding author; email: monosd{at}chop.edu
  • Abstract

    The human Major Histocompatibility Complex (MHC) is an approximately 4 Mb genomic segment on Chromosome 6 that plays a pivotal role in the immune response. Despite its importance in various traits and diseases, its complex nature makes it challenging to accurately characterize on a routine basis. We present a novel approach allowing targeted sequencing and de novo haplotypic assembly of the MHC region in heterozygous samples, using long-read sequencing technologies. Our approach is validated using two reference samples, two family trios, and an African-American sample. We achieved excellent coverage (96.6-99.9% with at least 30× depth) and high accuracy (99.89-99.99%) for the different haplotypes. This methodology offers a reliable and cost-effective method for sequencing and fully characterizing the MHC without the need for whole-genome sequencing, facilitating broader studies on this important genomic segment and having significant implications in immunology, genetics and medicine.

    • Received October 26, 2023.
    • Accepted September 19, 2024.

    This manuscript is Open Access.

    This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International license), as described at http://creativecommons.org/licenses/by-nc/4.0/.

    This article has not yet been cited by other articles.

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    1. Genome Res. gr.278588.123 Published by Cold Spring Harbor Laboratory Press

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