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Sample GSM3240142 Query DataSets for GSM3240142
Status Public on Mar 01, 2019
Title 6B4-Cap- replicate 1
Sample type SRA
 
Source name Microbial cell culture
Organism Pseudomonas [fluorescens] SBW25
Characteristics evolved strain: 6B4
morphotype: Switcher
Growth protocol Method: 3x single colonies of each of SBW25, 6A4 and 6B4 were grown on KB agar (28˚C, 48 hours), precultured in shaken KB (28˚C, overnight), grown to mid-exponential phase in shaken KB flasks (28˚C, OD600 of 0.4-0.6). SBW25 and 6A4 cultures were used for total RNA extraction; 6B4 cultures were split into cap+ and cap- fractions by centrifugation before total RNA isolation (and are included as separate samples above).
Extracted molecule total RNA
Extraction protocol RNA extraction and purification was performed using a RiboPureTM Bacteria Kit (Ambion®). RNA libraries were prepared for sequencing using standard Illumina protocols.
Normalized mRNA-seq library preparation was performed by the Australian Genome Research Facility (Brisbane, Australia). AGRF used a TruSeq kit to prep the RNA library, and perforemdd Ribo-Zero Bacteria rRNA Removal (https://sapac.illumina.com/products/scriptseq-bacteria.html). AGRF also performed the Illumina sequencing.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Data processing RNA-seq datasets were mapped to the SBW25 genome (downloaded from Genbank under the accession number NC_012660) via Bowtie2 with default settings
The coverage per gene of the genome mapping was determined with HTSeq. The gene annotation for HTSeq was also downloaded from the SBW25 Genbank entry.
Differentially expressed genes were identified by applying DESeq2. The standard workflow in https://bioconductor.org/packages/release/bioc/manuals/DESeq2/man/DESeq2.pdf was used, except that the alpha parameter was set to 0.3 to reduce the number of genes that were falsely classified as not significantly differentially expressed between the different morphotypes
Genome_build: ASM922v1
Supplementary_files_format_and_content: The processed data files contain information obtained by running "htseq-count" on the aligned sequence files. The files contain the sequence read coverage for each gene in the Pseudomonas fluorescens SBW25 genome. This data can be used to determine differentially expressed genes by for example DESeq2
 
Submission date Jul 02, 2018
Last update date Mar 01, 2019
Contact name Jenna Gallie
E-mail(s) [email protected]
Organization name Max Planck Institute for Evolutionary Biology
Street address August-Thienemann Strasse 2
City Ploen
ZIP/Postal code 24306
Country Germany
 
Platform ID GPL25322
Series (1)
GSE116490 RNA-seq data showing the effects of rpoD mutation t1682c in Pseudomonas fluorescens
Relations
BioSample SAMN09531954
SRA SRX4330075

Supplementary file Size Download File type/resource
GSM3240142_C7NA2ANXX-1719-06-2-1_L005.bam.txt.gz 26.5 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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