<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Leo Eberl</submitter><organism>Burkholderia cenocepacia</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-732</full_dataset_link><description>The purpose of this experiment was to determine differences in expression between wild-type B. cenocepacia H111 and two Tn5 mutants, R12 and R33, isolated during a Tn-mutagenesis screen for reduced pathogenicity.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Growth Protocol - Cells were grown  in LB at 37°C with shaking, to an OD600 of 2.7</sample_protocol><figure_sub>MIAME Score</figure_sub><figure_sub>Organization</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><figure_sub>Array Designs</figure_sub><data_protocol>Image Adquisition - Scan the washed and dried arrays as soon as possible using amicroarray scanner (G2565 BA, Agilent) and the Scan Control softwareversion A.7.0.3 Feb 2007 (Agilent).- Place the slides in the slide holder so that the numeric barcode isvisible.- Place the slides in the scanner, open the scan control software.- Scanner settings: scan region 61 x 21.6 mmscan resolution 5?m- Select Extended Dynamic Range with XDR Hi 100% and XDR Lo 10%(100% and 10% PMT gain).- Start the scan.- Every slide is scanned twice and two image files are generated: onewith the suffix 'H' and one with the suffix 'L'.- View the scanned images with the Feature Extraction software(Agilent).</data_protocol><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><study_type>transcription profiling by array</study_type><species>Burkholderia cenocepacia</species><pubmed_title>Exposing the Third Chromosome of Burkholderia cepacia complex Strains as a Virulence Plasmid</pubmed_title><pubmed_authors>Leo Eberl</pubmed_authors><pubmed_authors>K. Agnoli, S. Schwager, S. Uehlinger, A. Vergunst, D.F. Viteri, D.T. Nguyen, P.A. Sokol, A. Carlier and L. Eberl</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparison of H111 c3-null mutants R12 and R33 to wild-type</name><description>The purpose of this experiment was to determine differences in expression between wild-type B. cenocepacia H111 and two Tn5 mutants, R12 and R33, isolated during a Tn-mutagenesis screen for reduced pathogenicity.</description><dates><release>2012-07-11T00:00:00Z</release><modification>2022-03-07T00:26:25.901Z</modification><creation>2022-03-07T00:26:25.901Z</creation></dates><accession>E-MTAB-732</accession><cross_references><EFO>EFO_0002768</EFO></cross_references></HashMap>