|
Status |
Public on Oct 23, 2018 |
Title |
VRE untreated [13] |
Sample type |
SRA |
|
|
Source name |
Bacteria
|
Organism |
Enterococcus faecium |
Characteristics |
strain: RBWH1 agent: none
|
Treatment protocol |
Bacteria were grown in the presence or absense of PBT2 and zinc
|
Growth protocol |
Bacteria were grown in cation-adjusted Mueller-Hinton broth
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was isolated using the FastRNA® Pro Blue Kit (MP Biomedicals) and the SV Total RNA Isolation System (Promega) RNASeq analysis was performed at the Australian Genome Research Facility. The library was prepared using a Ribo-zero stranded protocol. Libraries were sequenced with a HiSeq 2500 ultra-high-throughput sequencing system (Illumina) to produce 100-base-paired end reads.
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
|
|
Description |
13
|
Data processing |
An average of 45 million reads per sample were generated and mapped to the reference genome using the 2-passmethod of the STAR aligner with default parameters. Duplicate reads were denoted with the MarkDuplicates tool of Picard (http://broadinstitute.github.io/picard) Differential gene expression was analysed using Degust (http://victorian-bioinformatics-438 consortium.github.io/degust/) genome build: Streptococcus pyogenes: NZ_AFRY01000001.1, Staphylococcus aureus: NC_007793.1, Enterococcus faecium: Bioproject PRJNA497960 Supplementary_files_format_and_content: xlsx files for each bacterial strain, CPM
|
|
|
Submission date |
Oct 22, 2018 |
Last update date |
Oct 23, 2018 |
Contact name |
Lisa Bohlmann |
E-mail(s) |
lisa_bo1@yahoo.de
|
Organization name |
University of Queensland
|
Street address |
University of Queensland
|
City |
St. Lucia |
ZIP/Postal code |
4072 |
Country |
Australia |
|
|
Platform ID |
GPL23589 |
Series (1) |
GSE121555 |
RNASeq analysis of untreated versus treated |
|
Relations |
BioSample |
SAMN10266256 |
SRA |
SRX4910581 |