“Matching” consent to purpose: The example of the Matchmaker Exchange

Stephanie O.M. Dyke, Bartha M. Knoppers, Ada Hamosh, Helen V. Firth, Matthew Hurles, Michael Brudno, Kym M. Boycott, Anthony A. Philippakis, Heidi L. Rehm

Research output: Contribution to journalArticlepeer-review

Abstract

The Matchmaker Exchange (MME) connects rare disease clinicians and researchers to facilitate the sharing of data from undiagnosed patients for the purpose of novel gene discovery. Such sharing raises the odds that two or more similar patients with candidate genes in common may be found, thereby allowing their condition to be more readily studied and understood. Consent considerations for data sharing in MME included both the ethical and legal differences between clinical and research settings and the level of privacy risk involved in sharing varying amounts of rare disease patient data to enable patient matches. In this commentary, we discuss these consent considerations and the resulting MME Consent Policy as they may be relevant to other international data sharing initiatives.

Original languageEnglish (US)
Pages (from-to)1281-1285
Number of pages5
JournalHuman mutation
Volume38
Issue number10
DOIs
StatePublished - Oct 2017

Keywords

  • consent
  • data access
  • data sharing
  • personalized medicine
  • precision medicine
  • privacy

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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