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Sample GSM4105660 Query DataSets for GSM4105660
Status Public on Apr 20, 2020
Title Sample 1B_RsmA_ChIPPAR
Sample type SRA
 
Source name RsmA_ChIPPAR
Organism Pseudomonas aeruginosa PAO1
Characteristics genotype/variation: RsmA-VSVG
cell type: Bacterial cells grown to OD 0.5
treatment protocol: sample taken prior to rifampicin treatment
chip antibody: Agarose-immobilized anti-VSVG (Sigma-Aldrich, Cat.# A1970, monoclonal antibody clone P5D4)
input/mock used: Sample 3_PAO1_midlog
Treatment protocol As indicated above, a subset of the samples were treated with rifampicin (150 µg/mL) for 30 minutes prior to the ChIP protocol,
Growth protocol Bacterial cultures were started from single colonies, grown overnight, and back-diluted in LB media
Extracted molecule genomic DNA
Extraction protocol DNA associated with proteins of interest were immunoprecipitated from lysates with anti-VSVG monocolonal antibody
Immunoprecipitated DNA was not size-selected during library construction
Libraries were prepared using NEBNext Ultra II DNA Library Prep Kit for Illumina (NEB) following manufacturer’s instructions.
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina HiSeq 2500
 
Data processing Paired ChIP-Seq reads corresponding to fragment sizes of either 200 or 400 bp (see SAMPLES section) were aligned to the PAO1 genome using bowtie2 (version 2.3.1) allowing 1 mismatch in a 28 bp seed region with no discordant or unpaired alignments.
The program samtools (version 1.2) was used to extract read 1 from each mapped read pair.
For the RsmA-V +/- rifampicin experiments (samples 1-2): Peaks were identified using QuEST (version 2.4; Valouev et al., 2008) using control data from exponential-phase wild-type cells (sample 3) with the following settings: KDE = 50, seeding fold enrichment = 1.25, extension fold enrichment = 1.5, ChIP to background fold enrichment = 2
For Hfq +/- ∆rsmAF (Samples 4 and 5) ChIP Experiment: Peaks were identified using QuEST (version 2.4; Valouev et al., 2008) using control data from log-phase wild-type cells (Sample 9) with the following settings: KDE = 45, seeding fold enrichment = 1.25, extension fold enrichment = 1.5, ChIP to background fold enrichment = 2.
For RsmA +/- ∆hfq (Samples 7 and 8) ChIP Experiment: Peaks were identified using QuEST (version 2.4; Valouev et al., 2008) using control data from log-phase wild-type cells (Sample 9) with the following settings: KDE = 30, seeding fold enrichment = 1.25, extension fold enrichment = 1.5, ChIP to background fold enrichment = 2.
Bed files for each experimental replicate were created by QuEST and the final processed bed files were generated by identifying the largest overlapping peak region which statisfy the following conditions: (1) peak regions must have a positive peak shift, (2) peak regions must have a positive strand correlation, (3) peak regions must have a q-value of less than 0.01, and (4) peak regions must be shared by two or more experimental replicates.
Genome_build: NC_002516.2
Supplementary_files_format_and_content: wig files were generated using QuEST; Scores represent normalized smoothed read density
Supplementary_files_format_and_content: bed intervals reflect regions with signicant (as defined above in data processing steps) enrichment of reads in the experimental condition in comparision to the mock control condition.
 
Submission date Oct 02, 2019
Last update date Apr 21, 2020
Contact name Michael J Gebhardt
Organization name University of Iowa
Department Department of Microbiology and Microbiology
Lab Gebhardt
Street address 431 Newton Road, 200A EMRB
City Iowa City
State/province IA
ZIP/Postal code 52242
Country USA
 
Platform ID GPL18782
Series (1)
GSE138338 Widespread targeting of nascent transcripts by RsmA in Pseudomonas aeruginosa
Relations
BioSample SAMN12898306
SRA SRX6938675

Supplementary file Size Download File type/resource
GSM4105660_RsmA_B_background_normalized.profile.wig.gz 21.3 Mb (ftp)(http) WIG
GSM4105660_RsmA_B_normalized.profile.wig.gz 22.4 Mb (ftp)(http) WIG
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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