dic(9;20) pediatric ALL with DNMT3B rearrangement - arrayCGH experiment
Array CGH derived copy number variations from dicentric chromosome dic(9;20) positive pediatric Acute lymphocytic leukemia B-lymphocyte samples, by utilizing an Agilent 400K SurePrint G3 Custom CGH Human Genome Microarray (e-Array design 84704)
- 27/07/2023
- 58 samples
- DAC: EGAC00001003324
- Technology: SurePrint G3 CGH
Access to sequencing reads is available by application to the "dic(9;20) pediatric ALL with DNMT3B rearrangement" study data access committee.
The "dic(9;20) pediatric ALL with DNMT3B rearrangement" study data access committee will consider applications for access to data sets stored in the European Genome-phenome Archive (EGA). Access to data will be granted to qualified researchers for appropriate use. A qualified researcher refers to a scientist who is employed, or a student enrolled at, or legitimately affiliated with an academic, non-profit or government institution, or a commercial company. Each application will be assessed to determine if: - It has been submitted by a qualified researcher or researchers, embedded in a recognised research institution that can provide institutional responsibility for appropriate research governance - The project described constitutes biomedical research in the context of the consent process; It breaches any of the ethical permissions or restrictions in the consent forms for any samples - It has the potential to produce information that will enable identification of individual participants
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.
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