| Literature DB >> 31256909 |
Kazutoyo Osoegawa1, Kalyan C Mallempati2, Sridevi Gangavarapu2, Arisa Oki3, Ketevan Gendzekhadze3, Susana R Marino4, Nicholas K Brown4, Maria P Bettinotti5, Eric T Weimer6, Gonzalo Montero-Martín7, Lisa E Creary7, Tamara A Vayntrub2, Chia-Jung Chang8, Medhat Askar9, Steven J Mack10, Marcelo A Fernández-Viña7.
Abstract
The 17th International HLA and Immunogenetics Workshop (IHIW) conducted a project entitled "The Study of Haplotypes in Families by NGS HLA". We investigated the HLA haplotypes of 1017 subjects in 263 nuclear families sourced from five US clinical immunogenetics laboratories, primarily as part of the evaluation of related donor candidates for hematopoietic stem cell and solid organ transplantation. The parents in these families belonged to five broad groups - African (72 parents), Asian (115), European (210), Hispanic (118) and "Other" (11). High-resolution HLA genotypes were generated for each subject using next-generation sequencing (NGS) HLA typing systems. We identified the HLA haplotypes in each family using HaplObserve, software that builds haplotypes in families by reviewing HLA allele segregation from parents to children. We calculated haplotype frequencies within each broad group, by treating the parents in each family as unrelated individuals. We also calculated standard measures of global linkage disequilibrium (LD) and conditional asymmetric LD for each ethnic group, and used untruncated and two-field allele names to investigate LD patterns. Finally we demonstrated the utility of consensus DNA sequences in identifying novel variants, confirming them using HLA allele segregation at the DNA sequence level.Entities:
Keywords: Family; HLA haplotype; Linkage disequilibrium
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Year: 2019 PMID: 31256909 PMCID: PMC6773484 DOI: 10.1016/j.humimm.2019.05.018
Source DB: PubMed Journal: Hum Immunol ISSN: 0198-8859 Impact factor: 2.850