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Exploring the current landscape of consumer genomics : proceedings of a workshop /

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자료유형E-Book
개인저자Hackmann, Meredith, rapporteur.
Addie, Siobhan, rapporteur.
Alper, Joe, rapporteur.
Beachy, Sarah H., rapporteur.
단체저자명National Academies of Sciences, Engineering, and Medicine (U.S.). Roundtable on Genomics and Precision Health,issuing body.
서명/저자사항Exploring the current landscape of consumer genomics :proceedings of a workshop /Meredith Hackmann, Siobhan Addie, Joe Alper, and Sarah H. Beachy, rapporteurs; Roundtable on Genomics and Precision Health, Board on Health Sciences Policy, Health and Medicine Division, The National Academies of Sciences, Engineering, Medicine.
발행사항Washington, DC : The National Academies Press, [2020]
형태사항1 online resource (1 PDF file (xix, 92 pages)) : illustrations
소장본 주기Master record variable field(s) change: 050, 082, 650 - OCLC control number change
ISBN

9780309673044
0309673046
9780309673068
0309673062
서지주기Includes bibliographical references.
내용주기Introduction and Workshop Overview -- Understanding Consumer Genomics Use -- Exploring the Role of Diversity and Health Disparities in Consumer Genomics -- Integration Within Scientific and Medical Communities -- Regulatory and Health Policy Issues -- How Can Consumer Genomics Be Better Integrated to Improve Health?
요약Consumer genomics, encompassing both direct-to-consumer applications (i.e., genetic testing that is accessed by a consumer directly from a commercial company apart from a health care provider) and consumer-driven genetic testing (i.e., genetic testing ordered by a health care provider in response to an informed patient request), has evolved considerably over the past decade, moving from more personal utility-focused applications outside of traditional health care to interfacing with clinical care in nontraditional ways. As consumer genomics has increasingly intersected with clinical applications, discussions have arisen around the need to demonstrate clinical and analytical validity and clinical utility due to the potential for misinterpretation by consumers. Clinical readiness and interest for this information have presented educational and training challenges for providers. At the same time, consumer genomics has emerged as a potentially innovative mechanism for thinking about health literacy and engaging participants in their health and health care. To explore the current landscape of consumer genomics and the implications for how genetic test information is used or may be used in research and clinical care, the Roundtable on Genomics and Precision Health of the National Academies of Sciences, Engineering, and Medicine hosted a public workshop on October 29, 2019, in Washington, DC. Discussions included such topics as the diversity of participant populations, the impact of consumer genomics on health literacy and engagement, knowledge gaps related to the use of consumer genomics in clinical care, and regulatory and health policy issues such as data privacy and security. A broad array of stakeholders took part in the workshop, including genomics and consumer genomics experts, epidemiologists, health disparities researchers, clinicians, users of consumer genomics research applications, representatives from patient advocacy groups, payers, bioethicists, regulators, and policy makers. This publication summarizes the presentations and discussion of the workshop.
기금정보주기This project was supported by contracts between the National Academy of Sciences and 23andMe; Air Force Medical Service (Contract No. FA8052-17-P-0007); American Academy of Nursing; American College of Medical Genetics and Genomics; American Medical Association; Association for Molecular Pathology; Biogen; Blue Cross and Blue Shield Association; College of American Pathologists; Color Genomics; Department of Veterans Affairs (Contract No. VA240-14-C-0037); Eisai Inc.; Geisinger; Genosity; Health Resources and Services Administration (Contract No. HHSH250201500001I/HHSH25034003T/0003); Helix; Illumina, Inc.; The Jackson Laboratory; Janssen Research & Development, LLC; Merck & Co., Inc. (Contract No. CMO-180815-002787); Myriad Women's Health; National Institutes of Health (Contract No. HHSN263201800029I/Order No. HHSN26300010): All of Us Research Program, National Cancer Institute, National Human Genome Research Institute, National Institute of Mental Health, National Institute of Nursing Research, National Institute on Aging, Office of Disease Prevention; National Society of Genetic Counselors; Pfizer Inc.; Regeneron; The University of Vermont Health Network Medical Group; and Vibrent Health. Any opinions, findings, conclusions, or recommendations expressed in this publication do not necessarily reflect the views of any organization or agency that provided support for the project.
회의명Exploring the Current Landscape of Consumer Genomics (Workshop)(2019 :Washington, D.C.)
일반주제명Genomics -- Congresses.
Human chromosome abnormalities -- Diagnosis -- Congresses.
Genomics
Human chromosome abnormalities -- Diagnosis
Genomics.
Genetic Testing.
Community Participation.
언어영어
기타형태 저록Print version:National Academies of Sciences, Engineering, and MedicineExploring the Current Landscape of Consumer Genomics : Proceedings of a WorkshopWashington, D.C. : National Academies Press,c20209780309673037
대출바로가기http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=2591576

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