<HashMap><database>biostudies-other</database><scores/><additional><submitter>Bekhouche I</submitter><pagination>e16950</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-ECPF-GEOD-23720</full_dataset_link><project>EurocanPlatform</project><abstract>Inflammatory breast cancer (IBC) is an aggressive form of BC poorly defined at the molecular level. We compared the molecular portraits of 63 IBC and 134 non-IBC (nIBC) clinical samples. Genomic imbalances of 49 IBCs and 124 nIBCs were determined using high-resolution array-comparative genomic hybridization, and mRNA expression profiles of 197 samples using whole-genome microarrays. Genomic profiles of IBCs were as heterogeneous as those of nIBCs, and globally relatively close. However, IBCs showed more frequent “complex” patterns and a higher percentage of genes with CNAs per sample. The number of altered regions was similar in both types, although some regions were altered more frequently and/or with higher amplitude in IBCs. Many genes were similarly altered in both types; however, more</abstract><repository>biostudies-other</repository><experiment_type>transcription profiling by array, comparative genomic hybridization by array</experiment_type><data_source>EurocanPlatform</data_source><omics_type>Unknown</omics_type><volume>6</volume><journal>PloS one</journal><species>Homo sapiens</species><pubmed_authors>Viens P</pubmed_authors><pubmed_authors>Bekhouche I</pubmed_authors><pubmed_authors>Charpin C</pubmed_authors><pubmed_authors>Birnbaum D</pubmed_authors><pubmed_authors>Houvenaeghel G</pubmed_authors><pubmed_authors>Bidaut G</pubmed_authors><pubmed_authors>Finetti P</pubmed_authors><pubmed_authors>Charafe-Jauffret E</pubmed_authors><pubmed_authors>Bertucci F</pubmed_authors><pubmed_authors>Tarpin C</pubmed_authors><pubmed_authors>Ferrari A</pubmed_authors><pubmed_authors>Chaffanet M</pubmed_authors><pubmed_authors>Adelaïde J</pubmed_authors><pubmed_authors>Jacquemier J</pubmed_authors></additional><is_claimable>false</is_claimable><name>High-resolution comparative genomic hybridization of inflammatory breast cancer and identification of candidate genes</name><description>Inflammatory breast cancer (IBC) is an aggressive form of BC poorly defined at the molecular level. We compared the molecular portraits of 63 IBC and 134 non-IBC (nIBC) clinical samples. Genomic imbalances of 49 IBCs and 124 nIBCs were determined using high-resolution array-comparative genomic hybridization, and mRNA expression profiles of 197 samples using whole-genome microarrays. Genomic profiles of IBCs were as heterogeneous as those of nIBCs, and globally relatively close. However, IBCs showed more frequent “complex” patterns and a higher percentage of genes with CNAs per sample. The number of altered regions was similar in both types, although some regions were altered more frequently and/or with higher amplitude in IBCs. Many genes were similarly altered in both types; however, more</description><dates><release>2016-04-14T13:46:46Z</release><publication>2011</publication><modification>2016-04-14T13:46:46Z</modification><creation>2016-04-14T13:46:46Z</creation></dates><accession>S-ECPF-GEOD-23720</accession><cross_references><GEO>GSE23720</GEO><ArrayExpress>E-GEOD-23720</ArrayExpress><EFO>EFO_0000635</EFO><EFO>EFO_0000305</EFO><ArrayExpress files>E-GEOD-23720</ArrayExpress files></cross_references></HashMap>