Data Access Policy of the HCEMM - Semmelweis University, Molecular Oncohematology Research Group

Donat Alpar
alpar.donat@med.semmelweis-univ.hu

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Dataset ID	Description	Technology	Samples
EGAD00001010878	In this study a next-generation sequencing based method was applied to comprehensively screen for recurrent, disease-relevant copy number aberrations in a cohort of Hungarian patients. Diagnostic bone marrow samples from 260 children with B-cell acute lymphoblastic leukemia as well as 72 control samples and were investigated by digital multiplex ligation-dependent probe amplification using the disease-specific D007 probemix. Whole chromosome gains and losses, as well as subchromosomal copy number aberrations were simultaneously profiled.	Illumina MiSeq	332