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Managing clinically significant findings in research: the UK10K example

Recent advances in sequencing technology allow data on the human genome to be generated more quickly and in greater detail than ever before. Such detail includes findings that may be of significance to the health of the research participant involved. Although research studies generally do not feed b...

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Autores principales: Kaye, Jane, Hurles, Matthew, Griffin, Heather, Grewal, Jasote, Bobrow, Martin, Timpson, Nic, Smee, Carol, Bolton, Patrick, Durbin, Richard, Dyke, Stephanie, Fitzpatrick, David, Kennedy, Karen, Kent, Alastair, Muddyman, Dawn, Muntoni, Francesco, Raymond, Lucy F, Semple, Robert, Spector, Tim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026295/
https://www.ncbi.nlm.nih.gov/pubmed/24424120
http://dx.doi.org/10.1038/ejhg.2013.290
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author Kaye, Jane
Hurles, Matthew
Griffin, Heather
Grewal, Jasote
Bobrow, Martin
Timpson, Nic
Smee, Carol
Bolton, Patrick
Durbin, Richard
Dyke, Stephanie
Fitzpatrick, David
Kennedy, Karen
Kent, Alastair
Muddyman, Dawn
Muntoni, Francesco
Raymond, Lucy F
Semple, Robert
Spector, Tim
author_facet Kaye, Jane
Hurles, Matthew
Griffin, Heather
Grewal, Jasote
Bobrow, Martin
Timpson, Nic
Smee, Carol
Bolton, Patrick
Durbin, Richard
Dyke, Stephanie
Fitzpatrick, David
Kennedy, Karen
Kent, Alastair
Muddyman, Dawn
Muntoni, Francesco
Raymond, Lucy F
Semple, Robert
Spector, Tim
author_sort Kaye, Jane
collection PubMed
description Recent advances in sequencing technology allow data on the human genome to be generated more quickly and in greater detail than ever before. Such detail includes findings that may be of significance to the health of the research participant involved. Although research studies generally do not feed back information on clinically significant findings (CSFs) to participants, this stance is increasingly being questioned. There may be difficulties and risks in feeding clinically significant information back to research participants, however, the UK10K consortium sought to address these by creating a detailed management pathway. This was not intended to create any obligation upon the researchers to feed back any CSFs they discovered. Instead, it provides a mechanism to ensure that any such findings can be passed on to the participant where appropriate. This paper describes this mechanism and the specific criteria, which must be fulfilled in order for a finding and participant to qualify for feedback. This mechanism could be used by future research consortia, and may also assist in the development of sound principles for dealing with CSFs.
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spelling pubmed-40262952014-09-01 Managing clinically significant findings in research: the UK10K example Kaye, Jane Hurles, Matthew Griffin, Heather Grewal, Jasote Bobrow, Martin Timpson, Nic Smee, Carol Bolton, Patrick Durbin, Richard Dyke, Stephanie Fitzpatrick, David Kennedy, Karen Kent, Alastair Muddyman, Dawn Muntoni, Francesco Raymond, Lucy F Semple, Robert Spector, Tim Eur J Hum Genet Article Recent advances in sequencing technology allow data on the human genome to be generated more quickly and in greater detail than ever before. Such detail includes findings that may be of significance to the health of the research participant involved. Although research studies generally do not feed back information on clinically significant findings (CSFs) to participants, this stance is increasingly being questioned. There may be difficulties and risks in feeding clinically significant information back to research participants, however, the UK10K consortium sought to address these by creating a detailed management pathway. This was not intended to create any obligation upon the researchers to feed back any CSFs they discovered. Instead, it provides a mechanism to ensure that any such findings can be passed on to the participant where appropriate. This paper describes this mechanism and the specific criteria, which must be fulfilled in order for a finding and participant to qualify for feedback. This mechanism could be used by future research consortia, and may also assist in the development of sound principles for dealing with CSFs. Nature Publishing Group 2014-09 2014-01-15 /pmc/articles/PMC4026295/ /pubmed/24424120 http://dx.doi.org/10.1038/ejhg.2013.290 Text en Copyright © 2014 Macmillan Publishers Limited http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Article
Kaye, Jane
Hurles, Matthew
Griffin, Heather
Grewal, Jasote
Bobrow, Martin
Timpson, Nic
Smee, Carol
Bolton, Patrick
Durbin, Richard
Dyke, Stephanie
Fitzpatrick, David
Kennedy, Karen
Kent, Alastair
Muddyman, Dawn
Muntoni, Francesco
Raymond, Lucy F
Semple, Robert
Spector, Tim
Managing clinically significant findings in research: the UK10K example
title Managing clinically significant findings in research: the UK10K example
title_full Managing clinically significant findings in research: the UK10K example
title_fullStr Managing clinically significant findings in research: the UK10K example
title_full_unstemmed Managing clinically significant findings in research: the UK10K example
title_short Managing clinically significant findings in research: the UK10K example
title_sort managing clinically significant findings in research: the uk10k example
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026295/
https://www.ncbi.nlm.nih.gov/pubmed/24424120
http://dx.doi.org/10.1038/ejhg.2013.290
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