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4478d6a6-51d9-490e-878d-a3e2c0ff3bd2 - samples

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https://www.omicsdi.org/dataset/ega/EGAD00001010878
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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.EGA dataset EGAD00001010878
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2023-05-22
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