Richter Syndrome targeted NGS (13 genes)
Targeted exome sequencing for a panel of 13 CLL driver genes
- 58 samples
- DAC: EGAC00001002237
- Technology: Illumina MiSeq
- HMB DUO:0000006 (version: 2019-01-07)health or medical or biomedical researchThis data use permission indicates that use is allowed for health/medical/biomedical purposes; does not include the study of population origins or ancestry.
- RS DUO:0000012 (version: 2019-01-07)research specific restrictionsThis data use modifier indicates that use is limited to studies of a certain research type.
- NPUNCU DUO:0000018 (version: 2019-01-07)not for profit, non commercial use onlyThis data use modifier indicates that use of the data is limited to not-for-profit organizations and not-for-profit use, non-commercial use.
- COL DUO:0000020 (version: 2019-01-07)collaboration requiredThis data use modifier indicates that the requestor must agree to collaboration with the primary study investigator(s).
- IRB DUO:0000021 (version: 2019-01-07)ethics approval requiredThis data use modifier indicates that the requestor must provide documentation of local IRB/ERB approval.
- PS DUO:0000027 (version: 2019-01-07)project specific restrictionThis data use modifier indicates that use is limited to use within an approved project.
- IS DUO:0000028 (version: 2019-01-07)institution specific restrictionThis data use modifier indicates that use is limited to use within an approved institution.
Policy for Data Access concerning the Richter Syndrome Project
Data Use Conditions: - DUO:0000006 (Primary Code) - DUO:00000012, DUO:00000018, DUO:00000020, DUO:00000021, DUO:00000027, DUO:00000028 (Secondary Codes) Policy motivation: The international biomedical research project on Richter Syndrome called « Genomic and Proteomic Study of Richter Syndrome » is recorded on clinicaltrials.gov under reference identifier NCT03619512 and is promoted by the University Hospital of Nancy, France. European high standards for patients’ data protection are required: storage in a secure database, with access granted after consideration to academic researchers and collaborators, and for non-profit institutions. Patient identification from genomic data is prohibited.
Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.
| Study ID | Study Title | Study Type |
|---|---|---|
| EGAS00001005495 | Other |
This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.