| Literature DB >> 26802209 |
Shana L McDevitt1, Jessen V Bredeson2, Scott W Roy3, Julie A Lane4, Janelle A Noble5.
Abstract
Next-generation sequencing (NGS) based HLA genotyping can generate PCR artifacts corresponding to IMGT/HLA Database alleles, for which multiple examples have been observed, including sequence corresponding to the HLA-DRB1(∗)03:42 allele. Repeat genotyping of 131 samples, previously genotyped as DRB1(∗)03:01 homozygotes using probe-based methods, resulted in the heterozygous call DRB1(∗)03:01+DRB1(∗)03:42. The apparent rare DRB1(∗)03:42 allele is hypothesized to be a "hybrid amplicon" generated by PCR crossover, a process in which a partial PCR product denatures from its template, anneals to a different allele template, and extends to completion. Unlike most PCR crossover products, "hybrid amplicons" always corresponds to an IMGT/HLA Database allele, necessitating a case-by-case analysis of whether its occurrence reflects the actual allele or is simply the result of PCR crossover. The Hybrid Amplicon/PCR Crossover Artifact Detector (HAPCAD) program mimics jumping PCR in silico and flags allele sequences that may also be generated as hybrid amplicon.Entities:
Keywords: Human Leukocyte Antigen; IMGT/HLA Database; Next-generation sequencing; Open-source tools; PCR crossovers
Mesh:
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Year: 2016 PMID: 26802209 PMCID: PMC4828336 DOI: 10.1016/j.humimm.2016.01.013
Source DB: PubMed Journal: Hum Immunol ISSN: 0198-8859 Impact factor: 2.850