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Single molecule real‐time DNA sequencing of HLA genes at ultra‐high resolution from 126 International HLA and Immunogenetics Workshop cell lines
Author(s) -
Turner T. R.,
Hayhurst J. D.,
Hayward D. R.,
Bultitude W. P.,
Barker D. J.,
Robinson J.,
Madrigal J. A.,
Mayor N. P.,
Marsh S. G. E.
Publication year - 2018
Publication title -
hla
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.347
H-Index - 99
eISSN - 2059-2310
pISSN - 2059-2302
DOI - 10.1111/tan.13184
Subject(s) - human leukocyte antigen , immunogenetics , genetics , biology , typing , hla b , haplotype , allele , major histocompatibility complex , zygosity , gene , computational biology , antigen
The hyperpolymorphic HLA genes play important roles in disease and transplantation and act as genetic markers of migration and evolution. A panel of 107 B‐lymphoblastoid cell lines (B‐LCLs) was established in 1987 at the 10th International Histocompatibility Workshop as a resource for the immunogenetics community. These B‐LCLs are well characterised and represent diverse ethnicities and HLA haplotypes. Here we have applied Pacific Biosciences’ Single Molecule Real‐Time (SMRT) DNA sequencing to HLA type 126 B‐LCL, including the 107 International HLA and Immunogenetics Workshop (IHIW) cells, to ultra‐high resolution. Amplicon sequencing of full‐length HLA class I genes (HLA‐A, ‐B and ‐C) and partial length HLA class II genes (HLA‐DRB1, ‐DQB1 and ‐DPB1) was performed. We typed a total of 931 HLA alleles, 895 (96%) of which were consistent with the typing in the IPD‐IMGT/HLA Database (Release 3.27.0, January 20, 2017), with 595 (64%) typed at a higher resolution. Discrepant types, including novel alleles ( n = 10) and changes in zygosity ( n = 13), as well as previously unreported types ( n = 34) were observed. In addition, patterns of linkage disequilibrium were distinguished by four‐field resolution typing of HLA‐B and HLA‐C. By improving and standardising the HLA typing of these B‐LCLs, we have ensured their continued usefulness as a resource for the immunogenetics community in the age of next generation DNA sequencing.