Targeted and complete genomic sequencing of the major histocompatibility complex in haplotypic form of individual heterozygous samples

Genome Res. 2024 Oct 29;34(10):1500-1513. doi: 10.1101/gr.278588.123.

Abstract

The human major histocompatibility complex (MHC) is a ∼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.

MeSH terms

  • Genome, Human
  • Haplotypes*
  • Heterozygote*
  • High-Throughput Nucleotide Sequencing / methods
  • Humans
  • Major Histocompatibility Complex* / genetics
  • Sequence Analysis, DNA / methods
  • Whole Genome Sequencing / methods