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- 2011278586 abstract "The initial sequencing of the human genome, carried out by an international group of experts, took 13 years and $2.7 billion to complete. In the decade since that achievement, sequencing technology has evolved at such a rapid pace that today a consumer can have his or her entire genome sequenced by a single company in a matter of days for less than $10,000, though the addition of interpretation may extend this time frame. Given the rapid technological advances, the potential effect on the lives of patients, and the increasing use of genomic information in clinical care, it is important to address how genomics data can be integrated into the clinical setting. Genetic tests are already used to assess the risk of breast and ovarian cancers, to diagnose recessive diseases such as cystic fibrosis, to determine drug dosages based on individual patient metabolism, and to identify therapeutic options for treating lung and breast tumors, melanoma, and leukemia. With these issues in mind and considering the potential impact that genomics information can have on the prevention, diagnosis, and treatment of disease, the Roundtable on Translating Genomic-Based Research for Health hosted a workshop on July 19, 2011, to highlight and identify the challenges and opportunities in integrating large-scale genomic information into clinical practice. Integrating large-scale genomic information into clinical practice summarizes the speaker presentations and the discussions that followed them. This report focuses on several key topics, including the analysis, interpretation, and delivery of genomic information plus workforce, ethical, and legal issues.".
- 2011278586 contributor B12166778.
- 2011278586 contributor B12166779.
- 2011278586 created "c2012.".
- 2011278586 date "2012".
- 2011278586 date "c2012.".
- 2011278586 dateCopyrighted "c2012.".
- 2011278586 description "Includes bibliographical references (p. 65-68).".
- 2011278586 description "Introduction -- The realization of genomic medicine -- The analysis of genomic data -- The interpretation of genomic data -- The delivery of genomic data -- Ethical and legal issues -- Workforce development -- Envisioning the future.".
- 2011278586 description "The initial sequencing of the human genome, carried out by an international group of experts, took 13 years and $2.7 billion to complete. In the decade since that achievement, sequencing technology has evolved at such a rapid pace that today a consumer can have his or her entire genome sequenced by a single company in a matter of days for less than $10,000, though the addition of interpretation may extend this time frame. Given the rapid technological advances, the potential effect on the lives of patients, and the increasing use of genomic information in clinical care, it is important to address how genomics data can be integrated into the clinical setting. Genetic tests are already used to assess the risk of breast and ovarian cancers, to diagnose recessive diseases such as cystic fibrosis, to determine drug dosages based on individual patient metabolism, and to identify therapeutic options for treating lung and breast tumors, melanoma, and leukemia. With these issues in mind and considering the potential impact that genomics information can have on the prevention, diagnosis, and treatment of disease, the Roundtable on Translating Genomic-Based Research for Health hosted a workshop on July 19, 2011, to highlight and identify the challenges and opportunities in integrating large-scale genomic information into clinical practice. Integrating large-scale genomic information into clinical practice summarizes the speaker presentations and the discussions that followed them. This report focuses on several key topics, including the analysis, interpretation, and delivery of genomic information plus workforce, ethical, and legal issues.".
- 2011278586 extent "xx, 92 p. :".
- 2011278586 hasFormat "Also available in Open Book format via the National Academies Press home page.".
- 2011278586 identifier "0309220343 (pbk.)".
- 2011278586 identifier "9780309220347 (pbk.)".
- 2011278586 identifier catalog.php?record_id=13256.
- 2011278586 isFormatOf "Also available in Open Book format via the National Academies Press home page.".
- 2011278586 issued "2012".
- 2011278586 issued "c2012.".
- 2011278586 language "eng".
- 2011278586 publisher "Washington, D.C. : National Academies Press,".
- 2011278586 relation "Also available in Open Book format via the National Academies Press home page.".
- 2011278586 spatial "United States".
- 2011278586 subject "Genomics Data processing Congresses.".
- 2011278586 subject "Genomics Practice United States Congresses.".
- 2011278586 subject "Genomics Research United States Congresses.".
- 2011278586 subject "Genomics.".
- 2011278586 subject "QH452.7 .I575 2012".
- 2011278586 tableOfContents "Introduction -- The realization of genomic medicine -- The analysis of genomic data -- The interpretation of genomic data -- The delivery of genomic data -- Ethical and legal issues -- Workforce development -- Envisioning the future.".
- 2011278586 title "Integrating large-scale genomic information into clinical practice : workshop summary / Steve Olson ... [et al.], rapporteurs ; Roundtable on Translating Genomic-Based Research for Health ; Board on Health Sciences Policy, Institute of Medicine of the National Academies.".
- 2011278586 type "text".