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Status |
Public on Apr 20, 2020 |
Title |
Sample 8B_RsmA_delhfq_ChIP |
Sample type |
SRA |
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Source name |
RsmA_delhfq_ChIP
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Organism |
Pseudomonas aeruginosa PAO1 |
Characteristics |
genotype/variation: RsmA-VSVG {delta}hfq cell type: Bacterial cells grown to OD 0.5 treatment protocol: no rifampicin treatment chip antibody: Agarose-immobilized anti-VSVG (Sigma-Aldrich, Cat.# A1970, monoclonal antibody clone P5D4) input/mock used: Sample 9_PAO1_3
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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,
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Growth protocol |
Bacterial cultures were started from single colonies, grown overnight, and back-diluted in LB media
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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.
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Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2500 |
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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.
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Submission date |
Oct 02, 2019 |
Last update date |
Apr 21, 2020 |
Contact name |
Michael J Gebhardt |
Organization name |
University of Iowa
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Department |
Department of Microbiology and Microbiology
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Lab |
Gebhardt
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Street address |
431 Newton Road, 200A EMRB
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City |
Iowa City |
State/province |
IA |
ZIP/Postal code |
52242 |
Country |
USA |
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Platform ID |
GPL18782 |
Series (1) |
GSE138338 |
Widespread targeting of nascent transcripts by RsmA in Pseudomonas aeruginosa |
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Relations |
BioSample |
SAMN12898310 |
SRA |
SRX6938692 |
Supplementary file |
Size |
Download |
File type/resource |
GSM4105677_RsmA-V_del_hfq_B_background_normalized.profile.wig.gz |
21.0 Mb |
(ftp)(http) |
WIG |
GSM4105677_RsmA-V_del_hfq_B_normalized.profile.wig.gz |
21.8 Mb |
(ftp)(http) |
WIG |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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