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Using de novo assembly to identify structural variation of eight complex immune system gene regions.
Zhang, Jia-Yuan; Roberts, Hannah; Flores, David S C; Cutler, Antony J; Brown, Andrew C; Whalley, Justin P; Mielczarek, Olga; Buck, David; Lockstone, Helen; Xella, Barbara; Oliver, Karen; Corton, Craig; Betteridge, Emma; Bashford-Rogers, Rachael; Knight, Julian C; Todd, John A; Band, Gavin.
Afiliação
  • Zhang JY; Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
  • Roberts H; Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
  • Flores DSC; Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
  • Cutler AJ; Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
  • Brown AC; Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
  • Whalley JP; Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
  • Mielczarek O; Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
  • Buck D; Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
  • Lockstone H; Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
  • Xella B; MRC Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, United Kingdom.
  • Oliver K; Wellcome Sanger Institute, Hinxton, Cambridge, United Kingdom.
  • Corton C; Wellcome Sanger Institute, Hinxton, Cambridge, United Kingdom.
  • Betteridge E; Wellcome Sanger Institute, Hinxton, Cambridge, United Kingdom.
  • Bashford-Rogers R; Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
  • Knight JC; Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
  • Todd JA; Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
  • Band G; Wellcome Centre for Human Genetics, University of Oxford, Oxford, United Kingdom.
PLoS Comput Biol ; 17(8): e1009254, 2021 08.
Article em En | MEDLINE | ID: mdl-34343164
Driven by the necessity to survive environmental pathogens, the human immune system has evolved exceptional diversity and plasticity, to which several factors contribute including inheritable structural polymorphism of the underlying genes. Characterizing this variation is challenging due to the complexity of these loci, which contain extensive regions of paralogy, segmental duplication and high copy-number repeats, but recent progress in long-read sequencing and optical mapping techniques suggests this problem may now be tractable. Here we assess this by using long-read sequencing platforms from PacBio and Oxford Nanopore, supplemented with short-read sequencing and Bionano optical mapping, to sequence DNA extracted from CD14+ monocytes and peripheral blood mononuclear cells from a single European individual identified as HV31. We use this data to build a de novo assembly of eight genomic regions encoding four key components of the immune system, namely the human leukocyte antigen, immunoglobulins, T cell receptors, and killer-cell immunoglobulin-like receptors. Validation of our assembly using k-mer based and alignment approaches suggests that it has high accuracy, with estimated base-level error rates below 1 in 10 kb, although we identify a small number of remaining structural errors. We use the assembly to identify heterozygous and homozygous structural variation in comparison to GRCh38. Despite analyzing only a single individual, we find multiple large structural variants affecting core genes at all three immunoglobulin regions and at two of the three T cell receptor regions. Several of these variants are not accurately callable using current algorithms, implying that further methodological improvements are needed. Our results demonstrate that assessing haplotype variation in these regions is possible given sufficiently accurate long-read and associated data. Continued reductions in the cost of these technologies will enable application of these methods to larger samples and provide a broader catalogue of germline structural variation at these loci, an important step toward making these regions accessible to large-scale genetic association studies.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article