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Mapping uncertainty in genomics

Bibliographic Data

ID12597604
AuthorsHeidi Howard (0000-0001-5256-7664, Uppsala University, corresponding author), Heidi Carmen Howard (0000-0001-6149-5498, Uppsala University), Erik Iwarsson (0000-0002-3827-0263, Department of Molecular Medicine and Surgery and Center for Molecular Medicine, Karolinska Institutet, CMM L8:02, Karolinska University Hospital, Stockholm, Sweden)
Year2017
Volume21
Issue2
Pages117-128
Publication date2017-08-22
Open AccessNo
TypeARTICLE
VenueJournal of Risk Research (JOURNAL)
Journal identifiersISSN: 1366-9877 • E-ISSN: 1466-4461
PublisherRoutledge (PUBLISHER • GB)
DOI10.1080/13669877.2016.1215344
OpenAlexW2750176470
LanguageEN
Citations received5
References cited23

The relatively novel and dynamic science of genomics holds many unknowns for stakeholders, and in particular for researchers and clinicians, as well as for participants and patients. At a time when many authors predict a future in which genomic medicine will be the norm, it is particularly relevant to discuss the unknowns surrounding genetics and genomics, including the notions of risk and uncertainty. This article will present a discussion regarding the uncertainty pertaining specifically to high throughput sequencing approaches, including the topic of incidental findings. This discussion will be guided by a taxonomy of uncertainty conceptualised around three areas of uncertainty: the source of uncertainty, the issues of uncertainty and the loci of uncertainty. This taxonomy can be used as a tool by all stakeholders involved in genomics to help further understand and anticipate uncertainties in genomics. Furthermore, to better contextualize this information, and also because this contribution is born out of an international project titled ‘Mind the Risk’, which addresses risk information in genetics and genomics from many different disciplinary perspectives, another aim of this article is to briefly present the basic issues pertaining to the unknowns, risks, and uncertainties of genetics as well as genomics for an audience of non-geneticists. Ultimately, the mapping out of uncertainty in genomics should allow for a better characterization of the uncertainty and consequently for a better management and communication of these uncertainties to end-users (research participants and patients)

Biology · Data science · Genome · Genomics · Precision medicine · BRCA gene mutations in cancer · Computer Science · CRISPR and Genetic Engineering · Genomics and Rare Diseases · Genetics

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    Open Access•Janneke M L Kuiper, Pascal Borry et al.•New Genetics and Society•2021

  • Communicating Scientific Uncertainty Across the Dissemination Trajectory

    Open Access•Chelsea L Ratcliff•Science Communication•2021

  • Uncertainty talk for bio-digital technologies

    Open Access•Gwendolyn Blue, Kristy Myles et al.•Environment and Planning E Nature…•2024

  • Varieties of Uncertainty in Health Care

    Open Access•Paul K J Han, William M P Klein et al.•Medical Decision Making•2011

  • ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

    Open Access•Robert C Green, Jonathan S Berg et al.•Genetics in Medicine•2013

  • A New Approach to Risk Evaluation and Management

    Open Access•Andreas Klinke, Ortwin Renn•Risk Analysis•2002

Citations per year0.63
Citation span2018 - 2024 (7)
Highly citedNo

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