{"id":"hum0168","version":1,"url":"https://humandbs.dbcls.jp/research/hum0168/v1","datePublished":"2019-11-08","versions":[{"version":1,"datePublished":"2019-11-08"}],"title":{"ja":"悪性腫瘍のゲノム・エピゲノム解析による病態解明","en":"Comprehensive genomic analyses of cancers"},"summary":{"aims":{"ja":"子宮腺筋症の原因遺伝子の探索","en":"Analysis of genetic background of adenomyosis"},"methods":{"ja":"子宮腺筋症の腺筋症病変部、併発内膜症病変部、併発筋腫病変部、周辺子宮筋層、腹水中単核球、末梢血から抽出したDNAを用いた全エクソン解析","en":"Whole exome sequencing was performed on fresh fronzen samples from adenomyosis individuals"},"targets":{"ja":"子宮腺筋症","en":"51 patients of adenomyosis"},"url":{"ja":null,"en":null}},"listingSummary":{"methods":{"ja":"配列決定","en":"Sequencing"},"targets":{"ja":"子宮腺筋症：51症例\n（日本人）","en":"51 adenomyosis patients\n(Japanese)"},"typeOfData":{"ja":"NGS\n（Exome）","en":"NGS\n(Exome)"}},"releaseNote":{"ja":"子宮腺筋症51症例の腺筋症病変部、併発内膜症病変部、併発筋腫病変部、周辺子宮筋層、腹水中単核球、末梢血から抽出したDNAを使用したExome解析の結果をbamファイルにて提供する。","en":"DNAs extracted from fresh fronzen samples from 51 adenomyosis ptients were used for the whole exome sequencing. Bam files are provided."},"dataProviders":[{"name":{"ja":"河津 正人","en":"Masahito Kawazu"},"organization":{"name":{"ja":"国立がん研究センター研究所","en":"National Cancer Center Research Institute"}}}],"researchProjects":[{"name":{"ja":"細胞情報学分野","en":"Division of Cellular Signaling"},"url":{"ja":null,"en":null}}],"grants":[{"title":{"ja":"LCM法による子宮腺筋症凍結検体の高感度遺伝子変異検出法の確立","en":"Establishment of highly sensitive SNV detection method of WES for uterine adenomyosis by LCM method."},"agency":{"ja":"科学研究費助成事業 基盤研究（C）","en":"KAKENHI Grant-in-Aid for Scientific Research (C)"},"grantIds":["19K07708"]}],"relatedPublications":[{"title":"Uterine adenomyosis is an oligoclonal disorder associated with KRAS mutations","doi":"https://doi.org/10.1038/s41467-019-13708-y","datasets":["JGAD000247"]}],"datasets":["JGAD000247"],"controlledAccessUsers":[]}