|
Status |
Public on Mar 04, 2019 |
Title |
RET_BWK |
Sample type |
SRA |
|
|
Source name |
Bacterial culture
|
Organism |
Escherichia coli |
Characteristics |
strain: BWK treatment: Retapamulin
|
Extracted molecule |
total RNA |
Extraction protocol |
Ribosome protected fragments were isolated as described in Oh et al. 2011 Libraries were generated as described in Oh et al. 2011
|
|
|
Library strategy |
OTHER |
Library source |
transcriptomic |
Library selection |
other |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
library strategy: Ribo-seq Reads were trimmed with Cutadapt 1.1.a Reads were first aligned to a ncRNA fasta file and the unmapped reads were subsequently mapped to the respective genomes with Bowtie 1.1.2 P-sites of the ribosomes were mapped as 15 nts away from the 3prime end of the read and used to calculate nucleotide rpm Genome_build: U00096, CP001509_3 Supplementary_files_format_and_content: wig, rpm values of the calculated ribosmal P-site
|
|
|
Submission date |
Nov 04, 2018 |
Last update date |
Oct 10, 2019 |
Contact name |
Alexander Mankin |
E-mail(s) |
shura@uic.edu
|
Organization name |
University of Illinois at Chicago
|
Department |
Pharmacognosy
|
Street address |
900 S. Ashland Avenue Room 3056
|
City |
Chicago |
State/province |
Illinois (IL) |
ZIP/Postal code |
60607 |
Country |
USA |
|
|
Platform ID |
GPL14548 |
Series (1) |
GSE122129 |
Retapamulin-assisted Ribo-seq reveals the alternative bacterial proteome |
|
Relations |
BioSample |
SAMN10373503 |
SRA |
SRX4976959 |