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Sample GSM1465035 Query DataSets for GSM1465035
Status Public on Mar 17, 2015
Title WT_RNA-Seq
Sample type SRA
 
Source name Culture cells
Organism Escherichia coli
Characteristics strain: K12-MG1693
growth phase: Exponential Phase
genotype: Wild-type
Growth protocol Overnight cultures from isolated colonies were diluted in fresh medium to an initial OD600~0.03 and grown to exponential phase (OD600~0.3) at 37ºC, with shaking at 200 rpm in Luria-Bertani (LB) medium supplemented with thymine (50 mg ml-1). When required, antibiotics were present at the following concentrations: kanamycin, 50 mg ml-1; tetracycline, 20 mg ml-1; streptomycin/spectinomycin 20 µg ml-1.
Extracted molecule total RNA
Extraction protocol RNA was isolated following cell lysis and phenol:chloroform extraction as previously described (Andrade, Pobre et al. 2012). After precipitation step in ethanol and 300 mM sodium acetate, RNA was resuspended in MilliQ-water. The integrity of RNA samples was evaluated by agarose gel electrophoresis. Turbo DNase (Ambion) treatment was used to remove contaminant DNA.
RNA libraries were prepared for sequencing by the company Vertis Biotechnologie AG in Germany
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Description Sample 1
Data processing Vertis Biotechnologie AG bioinformatics department did a preliminary analysis of the high-throughput sequencing results which included the mapping of the reads against E. coli genome (NC_000913 downloaded from NCBI genome database).
We then used the mapped files to run Cufflinks (estimates the relative abundance of the transcripts) and after Cuffdiff to find significant changes in transcript expression when comparing two samples (Trapnell, Williams et al. 2010).
Genome_build: ASM584v2
Supplementary_files_format_and_content: tab-delimited text files include RPKM values for each Sample …
 
Submission date Aug 05, 2014
Last update date May 15, 2019
Contact name Cecilia M. Arraiano
E-mail(s) [email protected]
Phone +351214469547
Organization name Instituto de Tecnologia Quimica e Biologica (ITQB) / Univ. Nova de Lisboa
Street address Av. Republica, Apt 127
City Oeiras
ZIP/Postal code 2781-901
Country Portugal
 
Platform ID GPL14548
Series (1)
GSE60107 Next generation sequencing analysis reveals that the ribonucleases RNase II, RNase R and PNPase affect bacterial motility and biofilm formation in E. coli
Relations
BioSample SAMN02952125
SRA SRX669653

Supplementary file Size Download File type/resource
GSM1465035_WT.txt.gz 91.8 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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