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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)

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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.

Study ID Study Title Study Type
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.

ID File Type Size Located in