<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Janos Demeter</submitter><organism>Salmonella enterica serovar Typhimurium</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-SMDB-3619</full_dataset_link><description>This experiment set includes all the input and spleen pooled arrays from the first negative selection passaged through 129SvJ mice and represents the 28-day timepoint.  "P.2 input" is the same thing as the P.1 output while "P.2 output" represents a sample of the 28-day output repassaged through mice for an additional 28 days.  Analysis demonstrated that there was no significant difference between the P.1 and P.2 re-passaged 28-day samples so they are treated the same.</description><repository>biostudies-arrayexpress</repository><figure_sub>MIAME Score</figure_sub><figure_sub>Raw Data</figure_sub><figure_sub>Organization</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><figure_sub>Array Designs</figure_sub><data_protocol>Feature Extraction - Title: Feature Extraction. Description: Software and parameters for feature extraction.</data_protocol><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><pubmed_abstract>A microarray-based negative selection screen was performed to identify Salmonella enterica serovar Typhimurium (serovar Typhimurium) genes that contribute to long-term systemic infection in 129X1/SvJ (Nramp1(r)) mice. A high-complexity transposon-mutagenized library was used to infect mice intraperitoneally, and the selective disappearance of mutants was monitored after 7, 14, 21, and 28 d postinfection. One hundred and eighteen genes were identified to contribute to serovar Typhimurium infection of the spleens of mice by 28 d postinfection. The negatively selected mutants represent many known aspects of Salmonella physiology and pathogenesis, although the majority of the identified genes are of putative or unknown function. Approximately 30% of the negatively selected genes correspond to </pubmed_abstract><study_type>transcription profiling by array</study_type><species>Salmonella enterica serovar Typhimurium</species><pubmed_title>Genome-Wide Screen for Salmonella Genes Required for Long-Term Systemic Infection of the Mouse.</pubmed_title><pubmed_authors>Janos Demeter</pubmed_authors><pubmed_authors>Kaman Chan</pubmed_authors><pubmed_authors>Trevor D. Lawley, Kaman Chan, Lucinda J. Thompson, Charles C. Kim, Gregory R. Govoni, Denise M. Monack</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transcription profiling of Salmonella passaged through 129SvJ mice to identify genes required for long term systemic infection</name><description>This experiment set includes all the input and spleen pooled arrays from the first negative selection passaged through 129SvJ mice and represents the 28-day timepoint.  "P.2 input" is the same thing as the P.1 output while "P.2 output" represents a sample of the 28-day output repassaged through mice for an additional 28 days.  Analysis demonstrated that there was no significant difference between the P.1 and P.2 re-passaged 28-day samples so they are treated the same.</description><dates><release>2006-06-06T00:00:00Z</release><modification>2022-02-04T01:23:22.148Z</modification><creation>2022-02-04T01:23:22.148Z</creation></dates><accession>E-SMDB-3619</accession><cross_references><pubmed>16518469</pubmed><EFO>EFO_0002768</EFO><doi>16518469</doi></cross_references></HashMap>