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| Status |
Public on Aug 10, 2021 |
| Title |
Base_ rep1 |
| Sample type |
SRA |
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| Source name |
bacteria
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| Organism |
Pseudomonas aeruginosa PAO1 |
| Characteristics |
treatment: untreated
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| 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).
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| Growth protocol |
A glycerol stock of pooled P. aeruginosa CTAGE library was thawed on ice and 1:1000 diluted into 100 mL LB medium.
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| 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).
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| Library strategy |
OTHER |
| Library source |
genomic |
| Library selection |
other |
| Instrument model |
HiSeq X Ten |
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| 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
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| Submission date |
Jan 13, 2021 |
| Last update date |
Aug 10, 2021 |
| Contact name |
ren zehui |
| E-mail(s) |
renzh6@mail2.sysu.edu.cn
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| Organization name |
SUN YAT-SEN UNIVERSITY
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| Street address |
No. 135, Xingang Xi Road
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| City |
Guangzhou |
| ZIP/Postal code |
510275 |
| Country |
China |
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| Platform ID |
GPL28604 |
| Series (1) |
| GSE164797 |
Targeted transposon screening in bacteria by CRISPR/Cas12k-guided transposase |
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| Relations |
| BioSample |
SAMN17311029 |
| SRA |
SRX9847220 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSM5019726_Base_1_insertion_umicounts.txt.gz |
121.2 Kb |
(ftp)(http) |
TXT |
SRA Run Selector |
| Raw data are available in SRA |
| Processed data provided as supplementary file |
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