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APPLaUD: access for patients and participants to individual level uninterpreted genomic data.

Adrian ThorogoodJason BobeBarbara PrainsackAnna MiddletonErick ScottSarah NelsonManuel CorpasNatasha BonhommeLaura Lyman RodriguezMadeleine MurtaghErika Kleidermannull null
Published in: Human genomics (2018)
Drawing on current practice and regulatory analysis, we outline legal, ethical, and practical guidance for genomic sequencing initiatives seeking to offer interested patients and participants access to their raw genomic data.
Keyphrases
  • end stage renal disease
  • ejection fraction
  • newly diagnosed
  • prognostic factors
  • peritoneal dialysis
  • electronic health record
  • big data
  • deep learning
  • genome wide