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The Matchmaker Exchange: a platform for rare disease gene discovery.
Philippakis, Anthony A; Azzariti, Danielle R; Beltran, Sergi; Brookes, Anthony J; Brownstein, Catherine A; Brudno, Michael; Brunner, Han G; Buske, Orion J; Carey, Knox; Doll, Cassie; Dumitriu, Sergiu; Dyke, Stephanie O M; den Dunnen, Johan T; Firth, Helen V; Gibbs, Richard A; Girdea, Marta; Gonzalez, Michael; Haendel, Melissa A; Hamosh, Ada; Holm, Ingrid A; Huang, Lijia; Hurles, Matthew E; Hutton, Ben; Krier, Joel B; Misyura, Andriy; Mungall, Christopher J; Paschall, Justin; Paten, Benedict; Robinson, Peter N; Schiettecatte, François; Sobreira, Nara L; Swaminathan, Ganesh J; Taschner, Peter E; Terry, Sharon F; Washington, Nicole L; Züchner, Stephan; Boycott, Kym M; Rehm, Heidi L.
Afiliação
  • Philippakis AA; The Broad Institute of Harvard and MIT, Cambridge, Massachusetts.
  • Azzariti DR; Department of Cardiology, Brigham & Women's Hospital, Boston, Massachusetts.
  • Beltran S; Harvard Medical School, Boston, Massachusetts.
  • Brookes AJ; Laboratory for Molecular Medicine, Partners Personalized Medicine, Boston, Massachusetts.
  • Brownstein CA; Centro Nacional de Análisis Genómico, Barcelona, Spain.
  • Brudno M; Department of Genetics, University of Leicester, Leicester, UK.
  • Brunner HG; Harvard Medical School, Boston, Massachusetts.
  • Buske OJ; Division of Genetics and Genomics and the Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts.
  • Carey K; Department of Computer Science, University of Toronto, Toronto, Canada.
  • Doll C; Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, Canada.
  • Dumitriu S; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada.
  • Dyke SO; Radboud University Medical Center, Department of Human Genetics, Nijmegen 6500 HB, The Netherlands.
  • den Dunnen JT; Maastricht University Medical Center, Department of Clinical Genetics, Maastricht 6202AZ, The Netherlands.
  • Firth HV; Department of Computer Science, University of Toronto, Toronto, Canada.
  • Gibbs RA; Genetics and Genome Biology Program, The Hospital for Sick Children, Toronto, Canada.
  • Girdea M; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada.
  • Gonzalez M; Gene Cloud, California.
  • Haendel MA; Google Inc, Mountain View, California.
  • Hamosh A; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada.
  • Holm IA; Centre of Genomics and Policy, Faculty of Medicine, McGill University, Quebec, Canada.
  • Huang L; Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Hurles ME; East Anglian Medical Genetics Service, Box 134, Cambridge University Hospitals NHS Foundation Trust, Cambridge Biomedical Campus, Cambridge CB2 0QQ, UK.
  • Hutton B; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, 77030.
  • Krier JB; Department of Computer Science, University of Toronto, Toronto, Canada.
  • Misyura A; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada.
  • Mungall CJ; The Genesis Project Inc, Miami, Florida.
  • Paschall J; Department of Medical Informatics and Clinical Epidemiology, Oregon Health & Science University, Portland, Oregon.
  • Paten B; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, Baltimore, Maryland.
  • Robinson PN; Harvard Medical School, Boston, Massachusetts.
  • Schiettecatte F; Division of Genetics and Genomics and the Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts.
  • Sobreira NL; The Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
  • Swaminathan GJ; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, CB10 1SA, UK.
  • Taschner PE; Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, CB10 1SA, UK.
  • Terry SF; Harvard Medical School, Boston, Massachusetts.
  • Washington NL; Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, 02115.
  • Züchner S; Centre for Computational Medicine, The Hospital for Sick Children, Toronto, Canada.
  • Boycott KM; Genomics Division, Lawrence Berkeley National Laboratory, Berkeley, California.
  • Rehm HL; European Molecular Biology Laboratory European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire, CB10 1SD, UK.
Hum Mutat ; 36(10): 915-21, 2015 Oct.
Article em En | MEDLINE | ID: mdl-26295439
There are few better examples of the need for data sharing than in the rare disease community, where patients, physicians, and researchers must search for "the needle in a haystack" to uncover rare, novel causes of disease within the genome. Impeding the pace of discovery has been the existence of many small siloed datasets within individual research or clinical laboratory databases and/or disease-specific organizations, hoping for serendipitous occasions when two distant investigators happen to learn they have a rare phenotype in common and can "match" these cases to build evidence for causality. However, serendipity has never proven to be a reliable or scalable approach in science. As such, the Matchmaker Exchange (MME) was launched to provide a robust and systematic approach to rare disease gene discovery through the creation of a federated network connecting databases of genotypes and rare phenotypes using a common application programming interface (API). The core building blocks of the MME have been defined and assembled. Three MME services have now been connected through the API and are available for community use. Additional databases that support internal matching are anticipated to join the MME network as it continues to grow.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Doenças Raras / Disseminação de Informação Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Predisposição Genética para Doença / Doenças Raras / Disseminação de Informação Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article