| Literature DB >> 29858803 |
Philip K Ehrenberg1, Aviva Geretz1,2, Rasmi Thomas3,4.
Abstract
The human leukocyte antigen (HLA) genes regulate and drive the immune system, and are among the most polymorphic loci in the human genome. HLA diversity is known to play an important role in transplantation and disease association studies. There are multiple approaches to DNA-based HLA genotyping and recent advances in next-generation sequencing (NGS) technologies have facilitated the development of whole gene sequencing methods. We describe an accurate, efficient, scalable, and cost-effective approach to contiguously amplify and sequence full-length genes of six HLA class I and II loci from 96 individuals on a single Illumina MiSeq run.Entities:
Keywords: Full-length amplification; HLA; HLA genotyping; Illumina; MIT-NGS; MiSeq; NGS; Next-generation sequencing
Mesh:
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Year: 2018 PMID: 29858803 DOI: 10.1007/978-1-4939-8546-3_6
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745