TY - JOUR
T1 - The challenges of the expanded availability of genomic information
T2 - an agenda-setting paper
AU - Borry, Pascal
AU - Bentzen, Heidi Beate
AU - Budin-Ljøsne, Isabelle
AU - Cornel, Martina C
AU - Howard, Heidi Carmen
AU - Feeney, Oliver
AU - Jackson, Leigh
AU - Mascalzoni, Deborah
AU - Mendes, Álvaro
AU - Peterlin, Borut
AU - Riso, Brigida
AU - Shabani, Mahsa
AU - Skirton, Heather
AU - Sterckx, Sigrid
AU - Vears, Danya
AU - Wjst, Matthias
AU - Felzmann, Heike
AU - Budin-Ljosne, Isabelle
PY - 2018/4
Y1 - 2018/4
N2 - Rapid advances in microarray and sequencing technologies are making genotyping and genome sequencing more affordable and readily available. There is an expectation that genomic sequencing technologies improve personalized diagnosis and personalized drug therapy. Concurrently, provision of direct-to-consumer genetic testing by commercial providers has enabled individuals' direct access to their genomic data. The expanded availability of genomic data is perceived as influencing the relationship between the various parties involved including healthcare professionals, researchers, patients, individuals, families, industry, and government. This results in a need to revisit their roles and responsibilities. In a 1-day agenda-setting meeting organized by the COST Action IS1303 "Citizen's Health through public-private Initiatives: Public health, Market and Ethical perspectives," participants discussed the main challenges associated with the expanded availability of genomic information, with a specific focus on public-private partnerships, and provided an outline from which to discuss in detail the identified challenges. This paper summarizes the points raised at this meeting in five main parts and highlights the key cross-cutting themes. In light of the increasing availability of genomic information, it is expected that this paper will provide timely direction for future research and policy making in this area.
AB - Rapid advances in microarray and sequencing technologies are making genotyping and genome sequencing more affordable and readily available. There is an expectation that genomic sequencing technologies improve personalized diagnosis and personalized drug therapy. Concurrently, provision of direct-to-consumer genetic testing by commercial providers has enabled individuals' direct access to their genomic data. The expanded availability of genomic data is perceived as influencing the relationship between the various parties involved including healthcare professionals, researchers, patients, individuals, families, industry, and government. This results in a need to revisit their roles and responsibilities. In a 1-day agenda-setting meeting organized by the COST Action IS1303 "Citizen's Health through public-private Initiatives: Public health, Market and Ethical perspectives," participants discussed the main challenges associated with the expanded availability of genomic information, with a specific focus on public-private partnerships, and provided an outline from which to discuss in detail the identified challenges. This paper summarizes the points raised at this meeting in five main parts and highlights the key cross-cutting themes. In light of the increasing availability of genomic information, it is expected that this paper will provide timely direction for future research and policy making in this area.
KW - Clinical and research genomic data
KW - Data sharing
KW - Direct-to-consumer genetic testing
KW - Genomics
KW - Informed consent
KW - Return of results
U2 - https://doi.org/10.1007/s12687-017-0331-7
DO - https://doi.org/10.1007/s12687-017-0331-7
M3 - Article
C2 - 28952070
SN - 1868-310X
VL - 9
SP - 103
EP - 116
JO - Journal of Community Genetics
JF - Journal of Community Genetics
IS - 2
ER -