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Sample GSM5019730 Query DataSets for GSM5019730
Status Public on Aug 10, 2021
Title IMP_ rep1
Sample type SRA
 
Source name bacteria
Organism Pseudomonas aeruginosa PAO1
Characteristics treatment: treated with imp
Treatment protocol The cells were treated for ~16h in the absence or in the presence of antibiotics (8 μg/mL imipenem, 1 μg/mL ceftazidime, and 1 μg/mL ofloxacin).
Growth protocol A glycerol stock of pooled P. aeruginosa CTAGE library was thawed on ice and 1:1000 diluted into 100 mL LB medium.
Extracted molecule genomic DNA
Extraction protocol The genomic DNA of each sample was extracted by the Ezup column bacteria genomic DNA purification kit (Sangon, Shanghai, China).
 
Library strategy OTHER
Library source genomic
Library selection other
Instrument model HiSeq X Ten
 
Data processing Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence
Sequenced reads filgered to find singal sequence
Sequenced reads were trimmed for adaptor sequence
mapped to whole genome using bowtie2
analysis insertion site with python program
Genome_build: GCF_000006765.1_ASM676v1_genomic
Supplementary_files_format_and_content: Matrix table with raw UMI counts for every insertion site and every sample
 
Submission date Jan 13, 2021
Last update date Aug 10, 2021
Contact name ren zehui
E-mail(s) renzh6@mail2.sysu.edu.cn
Organization name SUN YAT-SEN UNIVERSITY
Street address No. 135, Xingang Xi Road
City Guangzhou
ZIP/Postal code 510275
Country China
 
Platform ID GPL28604
Series (1)
GSE164797 Targeted transposon screening in bacteria by CRISPR/Cas12k-guided transposase
Relations
BioSample SAMN17311033
SRA SRX9847214

Supplementary file Size Download File type/resource
GSM5019730_IMP_1_insertion_umicounts.txt.gz 117.9 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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