Evidence map›Paper›PMID 22866951›Full record

ArticleBMC genomics2012

Ultra-high resolution HLA genotyping and allele discovery by highly multiplexed cDNA amplicon pyrosequencing.

Simon M Lank, Brittney A Golbach, Hannah M Creager, Roger W Wiseman, Derin B Keskin, Ellis L Reinherz, Vladimir Brusic, David H O'Connor

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Article in BMC genomics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

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21citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

8 authors.

Simon M LankWisconsin National Primate Research Center, University of Wisconsin-Madison, Madison, WI, USA.
Brittney A Golbach
Hannah M Creager
Roger W Wiseman
Derin B Keskin
Ellis L Reinherz
Vladimir Brusic
David H O'Connor

Funding

NIAID NIH HHS 4 U01 AI08959-02PHS HHS U01 A190043
6 · The paper itself

Abstract

backgroundHigh-resolution HLA genotyping is a critical diagnostic and research assay. Current methods rarely achieve unambiguous high-resolution typing without making population-specific frequency inferences due to a lack of locus coverage and difficulty in exon-phase matching. Achieving high-resolution typing is also becoming more challenging with traditional methods as the database of known HLA alleles increases.

resultsWe designed a cDNA amplicon-based pyrosequencing method to capture 94% of the HLA class I open-reading-frame with only two amplicons per sample, and an analogous method for class II HLA genes, with a primary focus on sequencing the DRB loci. We present a novel Galaxy server-based analysis workflow for determining genotype. During assay validation, we performed two GS Junior sequencing runs to determine the accuracy of the HLA class I amplicons and DRB amplicon at different levels of multiplexing. When 116 amplicons were multiplexed, we unambiguously resolved 99%of class I alleles to four- or six-digit resolution, as well as 100% unambiguous DRB calls. The second experiment, with 271 multiplexed amplicons, missed some alleles, but generated high-resolution, concordant typing for 93% of class I alleles, and 96% for DRB1 alleles. In a third, preliminary experiment we attempted to sequence novel amplicons for other class II loci with mixed success.

conclusionsThe presented assay is higher-throughput and higher-resolution than existing HLA genotyping methods, and suitable for allele discovery or large cohort sampling. The validated class I and DRB primers successfully generated unambiguously high-resolution genotypes, while further work is needed to validate additional class II genotyping amplicons.

Indexed as

Genes, MHC Class IGenes, MHC Class IISequence Analysis, DNAAllelesBase SequenceCell LineDNA, ComplementaryDNA PrimersGenotypeGenotyping TechniquesHigh-Throughput Nucleotide SequencingHLA AntigensHumansNucleic Acid Amplification TechniquesSequence AlignmentDNA, ComplementaryDNA PrimersHLA Antigens

Identifiers

PMID22866951
PMCPMC3575390

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.