Ethical, Legal and Social Implications in the Personal Genome Era
| Project/Area Number |
23613004
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
Bioethics
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| Research Institution | Shinshu University |
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Principal Investigator |
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| Co-Investigator(Kenkyū-buntansha) |
SAKURAI Akihiro 札幌医科大学, 医学部, 教授 (70262706)
WAKUI Keiko 信州大学, 医学部, 講師 (50324249)
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| Project Period (FY) |
2011 – 2013
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| Project Status |
Completed (Fiscal Year 2013)
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| Budget Amount *help |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2011: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
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| Keywords | パーソナルゲノム / 次世代シークエンサー / マイクロアレイ / 遺伝学的検査 / 遺伝カウンセリング / 遺伝子診断ビジネス / 偶発的所見 / マイクロアレイ染色体検査 |
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| Research Abstract |
We collected information of the following problems by participation to ESHG, ASHG and EAUHGS and document retrieval: 1) Bioethical issues on the personal genome analysis, 2) estimation methods for clinical utility and quality control of genetic testing, 3) Education or reporting methods of genetics or genomics to the public, students, and medical professionals. We translated the following two documents in order to design the Japanese system: 1) UK Genetic Testing Network: Review of commissioning arrangements for genetic services and strategic recommendations, 2) Eurogentest: A standardized framework for the validation and verification of clinical molecular genetic tests.
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Report
(4 results)
Research Products
(26 results)
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[Journal Article] Microarray and FISH-based genotype-phenotype analysis of 22 Japanese patients with Wolf-Hirschhorn syndrome.2013
Author(s)
Shimizu K, Wakui K, Kosho T, Okamoto N, Mizuno S, Itomi K, Hattori S, Nishio K, Samura O, Kobayashi Y, Kako Y, Arai T, Oh-Ishi T, Kawame H, Narumi Y, Ohashi H, Fukushima Y
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Journal Title
American Journal of Medical Genetics, Part A
Volume: 164A
Issue: 3
Pages: 597-609
DOI
Related Report
Peer Reviewed
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[Presentation] 疾病中心から患者中心の希少難治性疾患研究を可能とする患者支援団体と専門家集団とのネットワーク構築2012
Author(s)
福嶋義光, 松原洋一, 野村文夫, 斎藤加代子, 高田史男, 小杉眞司, 玉置知子, 櫻井晃洋, 関島良樹, 涌井敬子, 加藤光広, 小泉二郎
Organizer
日本人類遺伝学会第57回大会
Place of Presentation
幕張
Year and Date
2012-10-24
Related Report
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