Human lukocyte antigen (HLA) genotyping by next-generation sequencing: development of an in-house method and comparison with commercially available methods

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Title Human lukocyte antigen (HLA) genotyping by next-generation sequencing: development of an in-house method and comparison with commercially available methods
Publication Type thesis
School or College School of Medicine
Department Pathology
Author Profaizer, Tracie
Date 2017-08
Description Accurate genotyping of the human leukocyte antigens (HLA) are crucial for the success of hematopoietic stem cell and solid organ transplantation. Over the past 50 years, numerous methodologies have been used for HLA typing but technological limitations have prevented full interrogation of the HLA gene thus resulting in allelic ambiguity. In order to resolve these ambiguities, additional testing is often required, leading to increased expense and delay in reporting the genotyping results. Recently, advances in nucleic acid sequencing technologies, generally referred to as next-generation sequencing (NGS), have become available. HLA genotyping by NGS is poised to become the new gold standard for several reasons. First, the entire gene can be interrogated, as opposed to a few exons, thus enabling greater resolution of known polymorphisms outside of the T cell recognition site on the HLA molecule. Secondly, missing genetic sequences in the curated databases will become more complete thus improving the algorithms used for alignment to a reference sequence. Lastly, NGS will become the new gold standard because high-resolution genotyping can be achieved without the need for additional time and laboratory resources in order to resolve allelic ambiguities and meet typing requirements required by regulatory agencies. In this thesis I discuss my efforts to employ this new technology by developing an assay for genotyping of the HLA-A, B, C, DRB1, and DQB1 genes. In the new assay, 98% of all alleles typed correctly and unambiguously without the need for any secondary testing. This in-house method is later compared with two recently released commercial kits and 100% concordance was found between the three methods. Differences in workflow are compared and contrasted. In conclusion, we show that HLA genotyping by NGS produces more correct and unambiguous results than traditional Sanger sequencing without the need for reflex testing.
Type Text
Publisher University of Utah
Subject MESH Genotyping Techniques; Computational Biology; HLA Antigens; Alleles; Major Histocompatibility Complex; Polymerase Chain Reaction; High-Throughput Nucleotide Sequencing; Histocompatibility Testing; Sequence Analysis, DNA; Gene Library; Technology Transfer
Dissertation Institution University of Utah
Dissertation Name Master of Science
Language eng
Relation is Version of Digital version of Human Lukocyte Antigen (HLA) Genotyping by Next-Generation Sequencing: Development of an In-House Method and Comparison with Commercially Available Methods
Rights Management Copyright © Tracie Profaizer2017
Format application/pdf
Format Medium application/pdf
Source Original in Marriott Library Special Collections
ARK ark:/87278/s61c627v
Setname ir_etd
ID 1348634
Reference URL https://collections.lib.utah.edu/ark:/87278/s61c627v
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