Research ID
hum0024-v1Release info
Research title
Comprehensive Analysis of Genetic Alterations in Hematological Malignancies
Research overview
- Aims
- To perform a comprehensive analysis of genetic alterations of myelodysplastic syndromes (MDS) and related myeloid neoplasms (myelodysplasia).
- Methods
- Whole-exome sequencing of gDNAs extracted from leukemic cells and paired non-leukemic cells (Illumina Genome Analyzer IIx, HiSeq 2000, and HiSeq 2500).
- Participants/materials
- 13 MDSs and 1 chronic myelomonocytic leukemia (CMML) (leukemic cells and paired non-leukemic cells)
Datasets
| Cart | Dataset ID | Type of data | Analysis method | Access criteria | Date published |
|---|---|---|---|---|---|
| JGAD000023 | NGS (Exome) |
| Controlled-access (Type I) | 2020-09-28 |
Data provider
- Principal investigator
- Seishi Ogawa
- Affiliation
- Department of Pathology and Tumor Biology, Graduate School of Medicine, Kyoto University
Research projects
No research projects.
Grants
| Name | Title | Project number |
|---|---|---|
KAKENHI Grant-in-Aid for Scientific Research on Innovative Areas | システム的統合理解に基づくがんの先端的診断, 治療, 予防法の開発 |
|
KAKENHI Grant-in-Aid for Scientific Research (A) | Analysis on genetic basis of leukemia relapse and therapy resistance |
|
KAKENHI Grant-in-Aid for Young Scientists (B) | Exploring new gene target of 4q-UPD in Myelodysplastic syndromes |
|
New Energy and Industrial Technology Development Organization (NEDO) | 機能性アレルのデジタルカウントによる次世代"ExpressGenotype法"とその産業応用 |
|
Project for Development of Innovative Research on Cancer Therapeutics (P-DIRECT) | 骨髄異形成症候群におけるエピゲノム関連マーカーの探索と実用化 | N/A |
Health and Labour Science Research Grants from the Japanese Ministry of Health, Labour and Welfare, and Research on Measures for Intractable Disease | 不応性貧血の治癒率向上を目指した分子・免疫 病態研究 | N/A |
Cabinet Office, Government of Japan Funding Program for World-Leading Innovative R&D on Science and Technology (FIRST) | Development of medical technologies for treating intractable cancers and cardiovascular diseases | N/A |
Related publications
| Title | DOI | Dataset ID |
|---|---|---|
Frequent pathway mutations of splicing machinery in myelodysplasia. | ||
Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms. | ||
The landscape of somatic mutations in Down syndrome-related myeloid disorders. | ||
Landscape of genetic lesions in 944 patients with myelodysplastic syndromes. |
Controlled access users
No use of the controlled access data has been recorded.