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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/45949
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dc.contributor.authorAviva Geretzen_US
dc.contributor.authorPhilip K. Ehrenbergen_US
dc.contributor.authorAlain Bouckenoogheen_US
dc.contributor.authorMarcelo A. Fernández Viñaen_US
dc.contributor.authorNelson L. Michaelen_US
dc.contributor.authorDanaya Chansinghakuleen_US
dc.contributor.authorKriengsak Limkittikulen_US
dc.contributor.authorRasmi Thomasen_US
dc.contributor.otherStanford University School of Medicineen_US
dc.contributor.otherHJFen_US
dc.contributor.otherWalter Reed Army Institute of Researchen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherAsia-Pacific Clinical Developmenten_US
dc.contributor.otherAsia-Pacific Clinical Developmenten_US
dc.date.accessioned2019-08-23T11:17:00Z-
dc.date.available2019-08-23T11:17:00Z-
dc.date.issued2018-11-01en_US
dc.identifier.citationHuman Immunology. Vol.79, No.11 (2018), 773-780en_US
dc.identifier.issn18791166en_US
dc.identifier.issn01988859en_US
dc.identifier.other2-s2.0-85054032786en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85054032786&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/45949-
dc.description.abstract© 2018 The human leukocyte antigen (HLA) genes are highly variable and are known to play an important role in disease outcomes, including infectious diseases. Prior knowledge of HLA polymorphisms in a population usually forms the basis for an effective case-control study design. As a prelude to future disease association analyses, we report HLA class I and II diversity in 334 unrelated donors from a Dengue vaccine efficacy trial conducted in Thailand. Long-range PCR amplification of six HLA loci was performed on DNA extracted from saliva samples. HLA-A, -B, -C, -DPB1, -DQB1 and -DRB1 were genotyped using a next-generation sequencing method presented at the 17th International HLA and Immunogenetics Workshop. In total, we identified 201 HLA alleles, including 35 HLA-A, 57 HLA-B, 28 HLA-C, 24 HLA-DPB1, 21 HLA-DQB1 and 36 HLA-DRB1 alleles. Very common HLA alleles with frequencies greater than 10 percent were A∗11:01:01, A∗33:03:01, A∗24:02:01, B∗46:01:01, C∗07:02:01, C∗01:02:01, C∗08:01:01, DPB1∗05:01:01, DPB1∗13:01:01, DPB1∗04:01:01, DPB1∗02:01:02, DQB1∗03:01:01, DQB1∗05:02:01, DQB1∗03:03:02, DRB1∗12:02:01, DRB1∗09:01:02, and DRB1∗15:02:01. A novel HLA allele, B∗15:450, had a non-synonymous substitution and occurred in more than one donor. Population-based full-length NGS HLA typing is more conclusive and provides a sound foundation for exploring disease association in a given population.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85054032786&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleFull-length next-generation sequencing of HLA class I and II genes in a cohort from Thailanden_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1016/j.humimm.2018.09.005en_US
Appears in Collections:Scopus 2018

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