Copy Number Variations identified in 225 Diffuse Large B-Cell Lymphoma tumors

ABSTRACT: Copy Number Variations (CNVs) were identified performing Comparative Genomic Hybridization (CGH) on 225 patients after whole-genome amplification, using Agilent SurePrint G3 4x180K microarrays. CNVs were further integrated with gene expression (Affymetrix U133+2 arrays) and mutations (targeted DNA resequencing). Complete description of the methods, array quality checks and called segments are available as supplemental material in the corresponding publication.

ORGANISM(S): Homo sapiens

PROVIDER: GSE136962 | GEO | 2019/10/24

REPOSITORIES: GEO