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タイトル: Attitudes toward and current status of disclosure of secondary findings from next-generation sequencing: a nation-wide survey of clinical genetics professionals in Japan
著者: Tsuchiya, Mio
Yamada, Takahiro
Akaishi, Rina
Hamanoue, Haruka
Hirasawa, Akira
Hyodo, Maki
Imoto, Issei
Kosho, Tomoki
Kurosawa, Kenji
Murakami, Hiromi
Nakatani, Kaname
Nomura, Fumio
Sasaki, Aiko
Shimizu, Kenji
Tamai, Mariko
Umemura, Hiroshi
Watanabe, Atsushi
Yoshida, Akiko
Yoshihashi, Hiroshi
Yotsumoto, Junko
Kosugi, Shinji  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0001-6036-6491 (unconfirmed)
著者名の別形: 山田, 崇弘
小杉, 眞司
発行日: Dec-2020
出版者: Springer Nature
誌名: Journal of human genetics
巻: 65
開始ページ: 1045
終了ページ: 1053
抄録: The management of secondary findings (SFs), which are beyond the intended purpose of the analysis, from clinical comprehensive genomic analysis using next generation sequencing (NGS) presents challenges. Policy statements regarding their clinical management have been announced in Japan and other countries. In Japan, however, the current status of and attitudes of clinical genetics professionals toward reporting them are unclear. We conducted a questionnaire survey of clinical genetics professionals at two time points (2013 and 2019) to determine the enforcement of the SF management policy in cases of comprehensive genetic analysis of intractable diseases and clinical cancer genome profiling testing. According to the survey findings, 40% and 70% of the respondents stated in the 2013 and 2019 surveys, respectively, that they had an SF policy in the field of intractable diseases, indicating that SF policy awareness in Japan has changed significantly in recent years. Furthermore, a total of 80% of respondents stated that their facility had established a policy for clinical cancer genome profiling testing in the 2019 survey. In both surveys, the policies included the selection criteria for genes to be disclosed and the procedure to return SFs, followed by recommendations and proposals regarding SFs in Japan and other countries. To create a better list of the genes to be disclosed, further examination is needed considering the characteristics of each analysis.
著作権等: This is a post-peer-review, pre-copyedit version of an article published in 'Journal of human genetics'. The final authenticated version is available online at: https://doi.org/10.1038/s10038-020-0802-2
The full-text file will be made open to the public on 13 January 2021 in accordance with publisher's 'Terms and Conditions for Self-Archiving'.
This is not the published version. Please cite only the published version.
この論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。
URI: http://hdl.handle.net/2433/259189
DOI(出版社版): 10.1038/s10038-020-0802-2
PubMed ID: 32661284
出現コレクション:学術雑誌掲載論文等

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