• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Development of a hands-on cytogenetics training program for genomic medical workers

Research Project

Project/Area Number 17K00481
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Learning support system
Research InstitutionFujita Health University (2018-2019)
Shinshu University (2017)

Principal Investigator

KAWAMURA Rie  藤田医科大学, 総合医科学研究所, 助教 (20735534)

Co-Investigator(Kenkyū-buntansha) 涌井 敬子  信州大学, 学術研究院医学系, 講師 (50324249)
福嶋 義光  信州大学, 医学部, 特任教授 (70273084)
Project Period (FY) 2017-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2019: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2018: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2017: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywords遺伝学的検査 / 細胞遺伝 / cytogenetics / 遺伝医学 / 染色体検査 / 教材開発 / マイクロアレイ染色体検査
Outline of Final Research Achievements

We aimed to develop a hands-on training program to train medical workers, who can appropriately handle genomic information. The program was to properly interpret genomic information obtained from clinical cytogenetic testing. We set detailed goals, so that trainees could practice step-by-step, based on their ability and purpose. We made teaching materials that trainees could use it from their computers. After the training, based on their feedback, they wanted to continue with concrete practice. The outcome of this program shows, to enter the practical training was easier and would lead to human resource development for implementing genomic medicine.

Academic Significance and Societal Importance of the Research Achievements

全ゲノム解析でありながら形態学的検査であるために実習を受ける機会がほとんどない染色体核型分析などについて,具体的な染色体異常症例を通して細胞遺伝学的な評価法を学習できる実習プログラムを作成した.受講者に具体的な到達目標を示すことで,ゲノム医療従事者として必要な臨床細胞遺伝学のスキル取得と意識向上に繋がっていた.本実習プログラムを用いることで,受講者の認定資格取得の動機付けともなっており,ゲノム医療を実装するための人材育成へと繋がることが期待された.

Report

(4 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • 2017 Research-status Report
  • Research Products

    (7 results)

All 2020 2019 2018 2017

All Journal Article (1 results) (of which Peer Reviewed: 1 results) Presentation (6 results)

  • [Journal Article] A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia.2020

    • Author(s)
      Kawamura R, Kato T, Miyai S, Suzuki F, Naru Y, Kato M, Tanaka K, Nagasaka M, Tsutsumi M, Inagaki H, Ioroi T, Yoshida M, Nao T, Conlin LK, Iijima K, Kurahashi H, Taniguchi-Ikeda M.
    • Journal Title

      J Hum Genet.

      Volume: - Issue: 8 Pages: 705-709

    • DOI

      10.1038/s10038-020-0748-4

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed
  • [Presentation] 着床前診断を希望して来談されたクライエントの想いと遺伝カウンセリング2019

    • Author(s)
      河村理恵,森山育実,加藤麻希,河合美紀,宮井俊輔,倉橋浩樹
    • Organizer
      第43回日本遺伝カウンセリング学会学術集会
    • Related Report
      2019 Annual Research Report
  • [Presentation] dic(Y;22)と45,Xの核型をもつターナー症候群の一例2019

    • Author(s)
      河村理恵,稲垣秀人,山田緑,鈴木史彦,成悠希,倉橋浩樹
    • Organizer
      日本人類遺伝学会第64回大会
    • Related Report
      2019 Annual Research Report
  • [Presentation] Parthenogenetic maternalとdouble paternal alleleを有するキメラ症例の解析2019

    • Author(s)
      河村理恵,加藤武馬,宮井俊輔,鈴木史彦,成悠希,田中敬子,長坂美和子,池田真理子,倉橋浩樹
    • Organizer
      第41回日本小児遺伝学会学術集会
    • Related Report
      2018 Research-status Report
  • [Presentation] CNVs情報を基に選択したBACクローンのプローブミックスによる染色体分裂像多色FISH解析~複雑構造異常染色体・構造異常染色体モザイクの同定~2019

    • Author(s)
      涌井敬子,羽田明,朽方豊夢,水野誠司,古庄知己,福嶋義光
    • Organizer
      第41回日本小児遺伝学会学術集会
    • Related Report
      2018 Research-status Report
  • [Presentation] Report of a 46,XX/46,XY with parthenogenetic chimera2018

    • Author(s)
      河村理恵,加藤武馬,宮井俊輔,鈴木史彦,成悠希,田中敬子,長坂美和子,池田真理子,倉橋浩樹
    • Organizer
      日本人類遺伝学会第63回大会
    • Related Report
      2018 Research-status Report
  • [Presentation] マイクロアレイ染色体検査にて派生染色体に端部欠失が検出されなかった不均衡型転座症例2017

    • Author(s)
      河村理恵
    • Organizer
      日本人類遺伝学会第62回大会
    • Related Report
      2017 Research-status Report

URL: 

Published: 2017-04-28   Modified: 2021-02-19  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi