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A geographically matched control population efficiently limits the number of candidate disease-causing variants in an unbiased whole-genome analysis.
Rentoft, Matilda; Svensson, Daniel; Sjödin, Andreas; Olason, Pall I; Sjöström, Olle; Nylander, Carin; Osterman, Pia; Sjögren, Rickard; Netotea, Sergiu; Wibom, Carl; Cederquist, Kristina; Chabes, Andrei; Trygg, Johan; Melin, Beatrice S; Johansson, Erik.
Afiliação
  • Rentoft M; Department of Medical Biochemistry and Biophysics, Umeå University, SE Umeå, Sweden.
  • Svensson D; Computational Life Science Cluster, Department of Chemistry, Umeå University, SE Umeå, Sweden.
  • Sjödin A; Computational Life Science Cluster, Department of Chemistry, Umeå University, SE Umeå, Sweden.
  • Olason PI; Computational Life Science Cluster, Department of Chemistry, Umeå University, SE Umeå, Sweden.
  • Sjöström O; Division of CBRN Security and Defence, FOI-Swedish Defence Research Agency, SE Umeå, Sweden.
  • Nylander C; Science for Life Laboratory, Department of Cell and Molecular Biology, Uppsala University, SE Uppsala, Sweden.
  • Osterman P; Department of Radiation Sciences, Oncology, Umeå University, SE Umeå, Sweden.
  • Sjögren R; Unit of research, education and development, Region Jämtland Härjedalen, SE Östersund, Sweden.
  • Netotea S; Department of Radiation Sciences, Oncology, Umeå University, SE Umeå, Sweden.
  • Wibom C; Department of Medical Biochemistry and Biophysics, Umeå University, SE Umeå, Sweden.
  • Cederquist K; Computational Life Science Cluster, Department of Chemistry, Umeå University, SE Umeå, Sweden.
  • Chabes A; Computational Life Science Cluster, Department of Chemistry, Umeå University, SE Umeå, Sweden.
  • Trygg J; Science for Life Laboratory, Department of Biology and Biological Engineering, Chalmers University of Technology, SE Göteborg, Sweden.
  • Melin BS; Department of Radiation Sciences, Oncology, Umeå University, SE Umeå, Sweden.
  • Johansson E; Department of Medical Biosciences, Medical and Clinical Genetics, Umeå University, SE Umeå, Sweden.
PLoS One ; 14(3): e0213350, 2019.
Article em En | MEDLINE | ID: mdl-30917156
Whole-genome sequencing is a promising approach for human autosomal dominant disease studies. However, the vast number of genetic variants observed by this method constitutes a challenge when trying to identify the causal variants. This is often handled by restricting disease studies to the most damaging variants, e.g. those found in coding regions, and overlooking the remaining genetic variation. Such a biased approach explains in part why the genetic causes of many families with dominantly inherited diseases, in spite of being included in whole-genome sequencing studies, are left unsolved today. Here we explore the use of a geographically matched control population to minimize the number of candidate disease-causing variants without excluding variants based on assumptions on genomic position or functional predictions. To exemplify the benefit of the geographically matched control population we apply a typical disease variant filtering strategy in a family with an autosomal dominant form of colorectal cancer. With the use of the geographically matched control population we end up with 26 candidate variants genome wide. This is in contrast to the tens of thousands of candidates left when only making use of available public variant datasets. The effect of the local control population is dual, it (1) reduces the total number of candidate variants shared between affected individuals, and more importantly (2) increases the rate by which the number of candidate variants are reduced as additional affected family members are included in the filtering strategy. We demonstrate that the application of a geographically matched control population effectively limits the number of candidate disease-causing variants and may provide the means by which variants suitable for functional studies are identified genome wide.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Sequenciamento Completo do Genoma / Doenças Genéticas Inatas Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Suécia País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Sequenciamento Completo do Genoma / Doenças Genéticas Inatas Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: Europa Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Suécia País de publicação: Estados Unidos