<?xml version="1.0" encoding="ASCII"?>
<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">mouse</item><item key="factors"><item><item key="GSE7852GSM176892"/></item><item><item key="GSE7852GSM176893"/></item><item><item key="GSE7852GSM176897"/></item><item><item key="GSE7852GSM176899"/></item><item><item key="GSE7852GSM180519"/></item><item><item key="GSE7852GSM180531"/></item><item><item key="GSE7852GSM180533"/></item><item><item key="GSE7852GSM180536"/></item><item><item key="GSE7852GSM180538"/></item><item><item key="GSE7852GSM180540"/></item><item><item key="GSE7852GSM180542"/></item><item><item key="GSE7852GSM180544"/></item><item><item key="GSE7852GSM190555"/></item><item><item key="GSE7852GSM190556"/></item><item><item key="GSE7852GSM190562"/></item><item><item key="GSE7852GSM190563"/></item><item><item key="GSE7852GSM190564"/></item><item><item key="GSE7852GSM190565"/></item></item><item key="id">7849</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">Comparisons of global gene-expression profiles revealed a greater distinction between CD4+ Treg cells and CD4+ conventional (Tconv) T...</item><item key="geo_gse_id">E-GEOD-7852</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">18</item><item key="tags"><item>cell</item><item>spleen</item><item>thymus</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">transcription-profiling-of-mouse-fat-derived-flow</item><item key="geo_id_plat">E-GEOD-7852_A-AFFY-45</item><item key="name">Transcription profiling of mouse fat derived flow sorted Treg cells</item><item key="created">Nov.18, 2014</item><item key="summary">Comparisons of global gene-expression profiles revealed a greater distinction between CD4+ Treg cells and CD4+ conventional (Tconv) T cells  residing in abdominal (epidydimal) fat versus in more standard locations such as the spleen, thymus and LN. Experiment Overall Design: All gene expression profiles were obtained from highly purified T cell populations sorted by flow cytometry. To reduce variability, cells from multiple mice were pooled for sorting, and three replicates were generated for all groups. RNA from 3-5 x 104 cells was amplified, labeled, and hybridized to Affymetrix M430v2 microarrays. Raw data were preprocessed with the RMA algorithm in GenePattern, and averaged expression values were used for analysis.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-7852</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-7852/samples/</item></data></biogps>
