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AIRR community curation and standardised representation for immunoglobulin and T cell receptor germline sets.
Lees, William D; Christley, Scott; Peres, Ayelet; Kos, Justin T; Corrie, Brian; Ralph, Duncan; Breden, Felix; Cowell, Lindsay G; Yaari, Gur; Corcoran, Martin; Karlsson Hedestam, Gunilla B; Ohlin, Mats; Collins, Andrew M; Watson, Corey T; Busse, Christian E.
Afiliación
  • Lees WD; Institute of Structural and Molecular Biology, Birkbeck College, London, England.
  • Christley S; Human-Centered Computing and Information Science, Institute for Systems and Computer Engineering Technology and Science, Porto, Portugal.
  • Peres A; Peter O'Donnell Jr. School of Public Health, UT Southwestern Medical Center, Dallas, TX, USA.
  • Kos JT; Bioengineering Program, Faculty of Engineering, Bar-Ilan University, Ramat Gan, Israel.
  • Corrie B; Department of Biochemistry and Molecular Genetics, School of Medicine, University of Louisville, KY, USA.
  • Ralph D; Department of Biological Sciences, Simon Fraser University, Burnaby, BC, Canada.
  • Breden F; Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Cowell LG; Department of Biological Sciences, Simon Fraser University, Burnaby, BC, Canada.
  • Yaari G; Peter O'Donnell Jr. School of Public Health, Department of Immunology, School of Biomedical Sciences, UT Southwestern Medical Center, Dallas, TX, USA.
  • Corcoran M; Bioengineering Program, Faculty of Engineering, Bar-Ilan University, Ramat Gan, Israel.
  • Karlsson Hedestam GB; Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Swede.
  • Ohlin M; Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Swede.
  • Collins AM; Department of Immunotechnology and SciLifeLab, Lund University, Lund, Sweden.
  • Watson CT; School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney, NSW, Australia.
  • Busse CE; Department of Biochemistry and Molecular Genetics, School of Medicine, University of Louisville, KY, USA.
Article en En | MEDLINE | ID: mdl-37388275
Analysis of an individual's immunoglobulin or T cell receptor gene repertoire can provide important insights into immune function. High-quality analysis of adaptive immune receptor repertoire sequencing data depends upon accurate and relatively complete germline sets, but current sets are known to be incomplete. Established processes for the review and systematic naming of receptor germline genes and alleles require specific evidence and data types, but the discovery landscape is rapidly changing. To exploit the potential of emerging data, and to provide the field with improved state-of-the-art germline sets, an intermediate approach is needed that will allow the rapid publication of consolidated sets derived from these emerging sources. These sets must use a consistent naming scheme and allow refinement and consolidation into genes as new information emerges. Name changes should be minimised, but, where changes occur, the naming history of a sequence must be traceable. Here we outline the current issues and opportunities for the curation of germline IG/TR genes and present a forward-looking data model for building out more robust germline sets that can dovetail with current established processes. We describe interoperability standards for germline sets, and an approach to transparency based on principles of findability, accessibility, interoperability, and reusability.
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Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Immunoinformatics (Amst) Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Immunoinformatics (Amst) Año: 2023 Tipo del documento: Article País de afiliación: Reino Unido