GSE78041-GSM2065371-GPL21475-PMID_27748404.tsv
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SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) data_processing FastQ quality trimming using FastX (version 0.0.13) and a cut-off value of 20 PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) data_processing Fastq to fasta conversion using FastX FastX (version 0.0.13) PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) data_processing 5[linebreak] linker and poly A-tail removal using READemption PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) data_processing mapping of reads to E. coli O104:H4 rRNAs and tRNAs using READemption 0.3.7 and segemehl 0.2.0 PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) data_processing mapping of non-rRNA and tRNA reads to E. coli O104:H4 chromosome and plasmids using READemption 0.3.7 and segemehl 0.2.0 PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) data_processing generation of coverage graphs representing the number of pAA plasmid-associated mapped reads per nucleotide using READemption 0.3.7 PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) data_processing normalization of graphs to the total number of mapped reads per library using READemption 0.3.7 PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) data_processing Genome_build: NC_018658.1, NC_018659.1, NC_018660.1, NC_018666.1 PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) data_processing Supplementary_files_format_and_content: wig files representing the normalized number of pAA-associated mapped reads per nucleotide. Files contain wiggle-formatted files data for accessions NC_018658.1, NC_018659.1, NC_018660.1, and NC_018666.1. PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) extract_protocol Total RNA was extracted using the Trizol reagent (Thermo Fisher Scientific) and the concentration and purity of the samples were determined using Nano Drop. RNA integrity was monitored using the R6K ScreenTape system on the Agilent 2200 TapeStation. gDNA was removed by Turbo DNase (Thermo Fisher Scientific) in the presence of 1U/L RiboLock RNase Inhibitor (Thermo Fisher Scientific) for 60 min at 37°C. Following organic extraction (1x 25:24:1 v/v phenol/chloroform/ isoamyalcohol, 1x chloroform), RNA was recovered by overnight precipitation with 3 volumes of 30:1 100 % ethanol/3 M sodium acetate (pH 5.2). Next, the sample (TEX+) was depleted of processed RNAs using 1U per 1μg of RNA Terminator 5´-Phosphate-Dependent Exonuclease (TEX, Epicentre) in the presence of 1U/μL RNase Inhibitor for 60 min at 30° C. A control reaction without TEX (TEX-) was run in parallel. Following organic extraction, RNA was recovered by overnight precipitation and resuspended in RNase-free water. PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) extract_protocol cDNA libraries for the Illumina sequencing platform were constructed by vertis Biotechnology AG, Germany, as described previously (Berezikov et al.,2006), without the RNA size-fractionation step prior to cDNA synthesis. Briefly, RNA samples were polyA-tailed using polyA polymerase. Then, the 5[linebreak]-PPP termini were converted to 5[linebreak]-P using tobacco acid pyrophosphatase (TAP) to allow for the ligation of the 5’ end RNA adapter. First-strand cDNA was synthesized by an oligo(dT)-adapter primer and the M-MLV reverse transcriptase. In a PCR-based amplification step using a high fidelity DNA polymerase the cDNA concentration was increased to 20-30 ng/µl. A library-specific barcode for multiplex sequencing was part of a 3[linebreak]-sequencing adapter. PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) growth_protocol An overnight culture of E. coli O104:H4 strain LB226692 was diluted 1:10,000 in pre-warmed LB medium (10 g/L tryptone, 5 g/L yeast extract, 5 g/L NaCl) and cells were grown at 37oC, 180 rpm for 3.5 h to an OD600 of 0.52. PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) organism Escherichia coli O104:H4 PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) source_name exponentially growing cells PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) treatment_protocol 5 ml of cell suspension were added to 0.625 ml of pre-chilled stop solution (5 % phenol/95 % ethanol), vortexed and incubated for 5 min on ice. Cells were pelleted for 5 min at 5000 g, flash frozen in a dry ice-ethanol bath and stored at -80oC. PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) library_strategy RNA-Seq PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) characteristics strain: clinical isolate LB226692 PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) characteristics origin of isolation: patient with hemolytic uremic syndrome (HUS) PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) characteristics outbreak: 2011 outbreak centered in Northern Germany PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) growth_protocol An overnight culture of E. coli O104:H4 strain LB226692 was diluted 1:10,000 in pre-warmed LB medium (10 g/L tryptone, 5 g/L yeast extract, 5 g/L NaCl) and cells were grown at 37oC, 180 rpm for 3.5 h to an OD600 of 0.52. PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) organism Escherichia coli O104:H4 PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) source_name exponentially growing cells PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) treatment_protocol 5 ml of cell suspension were added to 0.625 ml of pre-chilled stop solution (5 % phenol/95 % ethanol), vortexed and incubated for 5 min on ice. Cells were pelleted for 5 min at 5000 g, flash frozen in a dry ice-ethanol bath and stored at -80oC. PGCGROWTHCONDITIONS
SRR3176282 GSE78041 GSM2065371 GPL21475 PMID_27748404 TEX-_E. coli O104:H4 Differential RNA-Seq (dRNA-seq) of Escherichia coli O104:H4 GPL21475: Illumina HiSeq 2500 (Escherichia coli O104:H4) contact_name Konrad,U.,Förstner PGCGROWTHCONDITIONS