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How do consent forms for diagnostic high‐throughput sequencing address unsolicited and secondary findings? A content analysis
Author(s) -
Vears D.F.,
Niemiec E.,
Howard H.C.,
Borry P.
Publication year - 2018
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.13391
Subject(s) - terminology , exome sequencing , informed consent , variety (cybernetics) , medicine , exome , family medicine , psychology , alternative medicine , computer science , biology , genetics , pathology , philosophy , linguistics , artificial intelligence , mutation , gene
Graphical representation of the categories and subcategories identified in the forms. † Value includes 13 forms that did not mention unsolicited findings (UF) and/or secondary findings (SF).
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