Genome-based diagnostics :: clarifying pathways to clinical use : workshop summary /
The Roundtable on Translating Genomic-Based Research for Health held a follow-up workshop on November 15, 2011 titled Facilitating Development and Utilization of Genome-Based Diagnostic Technologies to further explore the differences in evidence required for clinical use, regulatory oversight, guide...
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| Format: | Elektronisch Tagungsbericht E-Book |
| Sprache: | English |
| Veröffentlicht: |
Washington, D.C. :
National Academies Press,
©2012.
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| Schlagworte: | |
| Online-Zugang: | Volltext |
| Zusammenfassung: | The Roundtable on Translating Genomic-Based Research for Health held a follow-up workshop on November 15, 2011 titled Facilitating Development and Utilization of Genome-Based Diagnostic Technologies to further explore the differences in evidence required for clinical use, regulatory oversight, guideline inclusion, coverage, and reimbursement of genomic diagnostic tests among stakeholders with the goal of clarifying a pathway for successfully bringing tests to clinical use for the benefit of patients. Presenters at the workshop were asked to consider four broad issues:1. How are the barriers to successful genomic test development viewed?2. What are potential solutions?3. What are the obstacles to achieving those solutions?4. How can those obstacles be overcome? |
| Beschreibung: | Title from PDF title page (viewed October 26, 2012). |
| Beschreibung: | 1 online resource (1 PDF file (xx, 83 pages) : illustrations |
| Bibliographie: | Includes bibliographical references. |
| ISBN: | 9780309253949 0309253942 9780309253956 0309253950 1283636298 9781283636292 0309253977 9780309253970 |
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| 520 | 3 | |a The Roundtable on Translating Genomic-Based Research for Health held a follow-up workshop on November 15, 2011 titled Facilitating Development and Utilization of Genome-Based Diagnostic Technologies to further explore the differences in evidence required for clinical use, regulatory oversight, guideline inclusion, coverage, and reimbursement of genomic diagnostic tests among stakeholders with the goal of clarifying a pathway for successfully bringing tests to clinical use for the benefit of patients. Presenters at the workshop were asked to consider four broad issues:1. How are the barriers to successful genomic test development viewed?2. What are potential solutions?3. What are the obstacles to achieving those solutions?4. How can those obstacles be overcome? | |
| 500 | |a Title from PDF title page (viewed October 26, 2012). | ||
| 505 | 0 | |a Introduction -- Calls for Change -- Test Developers -- Patients -- Payers -- Regulation, Reimbursement, and Public Health -- Discussion of Major Proposals -- References -- Appendix A: Workshop Agenda -- Appendix B: Speaker Biographical Sketches -- Appendix C: Statement of Task -- Appendix D: Registered Attendees. | |
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| contents | Introduction -- Calls for Change -- Test Developers -- Patients -- Payers -- Regulation, Reimbursement, and Public Health -- Discussion of Major Proposals -- References -- Appendix A: Workshop Agenda -- Appendix B: Speaker Biographical Sketches -- Appendix C: Statement of Task -- Appendix D: Registered Attendees. |
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Berger, rapporteurs ; Roundtable on Translating Genomic-Based Research for Health, Board on Health Sciences Policy, Institute of Medicine of the National Academies.</subfield></datafield><datafield tag="260" ind1=" " ind2=" "><subfield code="a">Washington, D.C. :</subfield><subfield code="b">National Academies Press,</subfield><subfield code="c">©2012.</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 online resource (1 PDF file (xx, 83 pages) :</subfield><subfield code="b">illustrations</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">computer</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">online resource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="340" ind1=" " ind2=" "><subfield code="g">polychrome.</subfield><subfield code="2">rdacc</subfield><subfield code="0">http://rdaregistry.info/termList/RDAColourContent/1003</subfield></datafield><datafield tag="347" ind1=" " ind2=" "><subfield code="a">data file</subfield></datafield><datafield tag="504" ind1=" " ind2=" "><subfield code="a">Includes bibliographical references.</subfield></datafield><datafield tag="520" ind1="3" ind2=" "><subfield code="a">The Roundtable on Translating Genomic-Based Research for Health held a follow-up workshop on November 15, 2011 titled Facilitating Development and Utilization of Genome-Based Diagnostic Technologies to further explore the differences in evidence required for clinical use, regulatory oversight, guideline inclusion, coverage, and reimbursement of genomic diagnostic tests among stakeholders with the goal of clarifying a pathway for successfully bringing tests to clinical use for the benefit of patients. 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| spelling | Genome-based diagnostics : clarifying pathways to clinical use : workshop summary / Steve Olson and Adam C. Berger, rapporteurs ; Roundtable on Translating Genomic-Based Research for Health, Board on Health Sciences Policy, Institute of Medicine of the National Academies. Washington, D.C. : National Academies Press, ©2012. 1 online resource (1 PDF file (xx, 83 pages) : illustrations text txt rdacontent computer c rdamedia online resource cr rdacarrier polychrome. rdacc http://rdaregistry.info/termList/RDAColourContent/1003 data file Includes bibliographical references. The Roundtable on Translating Genomic-Based Research for Health held a follow-up workshop on November 15, 2011 titled Facilitating Development and Utilization of Genome-Based Diagnostic Technologies to further explore the differences in evidence required for clinical use, regulatory oversight, guideline inclusion, coverage, and reimbursement of genomic diagnostic tests among stakeholders with the goal of clarifying a pathway for successfully bringing tests to clinical use for the benefit of patients. Presenters at the workshop were asked to consider four broad issues:1. How are the barriers to successful genomic test development viewed?2. What are potential solutions?3. What are the obstacles to achieving those solutions?4. How can those obstacles be overcome? Title from PDF title page (viewed October 26, 2012). Introduction -- Calls for Change -- Test Developers -- Patients -- Payers -- Regulation, Reimbursement, and Public Health -- Discussion of Major Proposals -- References -- Appendix A: Workshop Agenda -- Appendix B: Speaker Biographical Sketches -- Appendix C: Statement of Task -- Appendix D: Registered Attendees. English. Human chromosome abnormalities Diagnosis United States Congresses. Genetic disorders Diagnosis United States Congresses. Genetic Testing standards Genomics standards https://id.nlm.nih.gov/mesh/D023281Q000592 United States https://id.nlm.nih.gov/mesh/D014481 Chromosomes humains Anomalies Diagnostic États-Unis Congrès. Maladies génétiques Diagnostic États-Unis Congrès. SCIENCE Life Sciences Genetics & Genomics. bisacsh Genetic disorders Diagnosis fast Human chromosome abnormalities Diagnosis fast United States fast https://id.oclc.org/worldcat/entity/E39PBJtxgQXMWqmjMjjwXRHgrq Congress proceedings (reports) aat Conference papers and proceedings fast Conference papers and proceedings. lcgft http://id.loc.gov/authorities/genreForms/gf2014026068 Actes de congrès. rvmgf Olson, Steve, 1956- https://id.oclc.org/worldcat/entity/E39PBJpV6yX9jFKMQMYFvVkhpP Berger, Adam C. http://id.loc.gov/authorities/names/no2010177254 Institute of Medicine (U.S.). Roundtable on Translating Genomic-Based Research for Health. http://id.loc.gov/authorities/names/no2008119550 Facilitating Development and Utilization of Genome-Based Diagnostic Technologies: A Workshop (2011 : Washington, D.C.) http://id.loc.gov/authorities/names/n2012189334 has work: Genome-based diagnostics (Text) https://id.oclc.org/worldcat/entity/E39PCFtFF7gq3qYThCpwYyTQ4m https://id.oclc.org/worldcat/ontology/hasWork Print version: Washington, D.C. : National Academies Press, 2012 9780309253949 FWS01 ZDB-4-EBA FWS_PDA_EBA https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=476039 Volltext |
| spellingShingle | Genome-based diagnostics : clarifying pathways to clinical use : workshop summary / Introduction -- Calls for Change -- Test Developers -- Patients -- Payers -- Regulation, Reimbursement, and Public Health -- Discussion of Major Proposals -- References -- Appendix A: Workshop Agenda -- Appendix B: Speaker Biographical Sketches -- Appendix C: Statement of Task -- Appendix D: Registered Attendees. Human chromosome abnormalities Diagnosis United States Congresses. Genetic disorders Diagnosis United States Congresses. Genetic Testing standards Genomics standards https://id.nlm.nih.gov/mesh/D023281Q000592 Chromosomes humains Anomalies Diagnostic États-Unis Congrès. Maladies génétiques Diagnostic États-Unis Congrès. SCIENCE Life Sciences Genetics & Genomics. bisacsh Genetic disorders Diagnosis fast Human chromosome abnormalities Diagnosis fast |
| subject_GND | https://id.nlm.nih.gov/mesh/D023281Q000592 https://id.nlm.nih.gov/mesh/D014481 http://id.loc.gov/authorities/genreForms/gf2014026068 |
| title | Genome-based diagnostics : clarifying pathways to clinical use : workshop summary / |
| title_auth | Genome-based diagnostics : clarifying pathways to clinical use : workshop summary / |
| title_exact_search | Genome-based diagnostics : clarifying pathways to clinical use : workshop summary / |
| title_full | Genome-based diagnostics : clarifying pathways to clinical use : workshop summary / Steve Olson and Adam C. Berger, rapporteurs ; Roundtable on Translating Genomic-Based Research for Health, Board on Health Sciences Policy, Institute of Medicine of the National Academies. |
| title_fullStr | Genome-based diagnostics : clarifying pathways to clinical use : workshop summary / Steve Olson and Adam C. Berger, rapporteurs ; Roundtable on Translating Genomic-Based Research for Health, Board on Health Sciences Policy, Institute of Medicine of the National Academies. |
| title_full_unstemmed | Genome-based diagnostics : clarifying pathways to clinical use : workshop summary / Steve Olson and Adam C. Berger, rapporteurs ; Roundtable on Translating Genomic-Based Research for Health, Board on Health Sciences Policy, Institute of Medicine of the National Academies. |
| title_short | Genome-based diagnostics : |
| title_sort | genome based diagnostics clarifying pathways to clinical use workshop summary |
| title_sub | clarifying pathways to clinical use : workshop summary / |
| topic | Human chromosome abnormalities Diagnosis United States Congresses. Genetic disorders Diagnosis United States Congresses. Genetic Testing standards Genomics standards https://id.nlm.nih.gov/mesh/D023281Q000592 Chromosomes humains Anomalies Diagnostic États-Unis Congrès. Maladies génétiques Diagnostic États-Unis Congrès. SCIENCE Life Sciences Genetics & Genomics. bisacsh Genetic disorders Diagnosis fast Human chromosome abnormalities Diagnosis fast |
| topic_facet | Human chromosome abnormalities Diagnosis United States Congresses. Genetic disorders Diagnosis United States Congresses. Genetic Testing standards Genomics standards United States Chromosomes humains Anomalies Diagnostic États-Unis Congrès. Maladies génétiques Diagnostic États-Unis Congrès. SCIENCE Life Sciences Genetics & Genomics. Genetic disorders Diagnosis Human chromosome abnormalities Diagnosis Congress proceedings (reports) Conference papers and proceedings Conference papers and proceedings. Actes de congrès. |
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