|
| Status |
Public on Oct 15, 2022 |
| Title |
Control_3, biological replicate3 |
| Sample type |
SRA |
| |
|
| Source name |
Exponential phase bacterial culture of Staphylococcus aureus
|
| Organism |
Staphylococcus aureus |
| Characteristics |
treatment: Staphylococcus aureus strain in liquid LB medium
growth phase: Exponential phase
genotype: wild type
|
| Treatment protocol |
Bacterial cells were collected and kept on ice to extract RNA.
|
| Growth protocol |
Bacterial cells were grown for 12 hr at 37C.
|
| Extracted molecule |
total RNA |
| Extraction protocol |
Trizol extraction of total RNA was performed according to the manufacturer's instructions.
RNA-seq strand-specific libraries were prepared following TruSeq RNA sample preparation Kit from Illumina (San Diego, CA), using 5 μg of total RNA. Briefly, rRNA was removed by RiboZero rRNA removal kit (Epicenter), fragmented using fragmentation buffer. cDNA synthesis, end repair, A-base addition and ligation of the Illumina-indexed adaptors were performed according to Illumina’s protocol. Libraries were then size selected for cDNA target fragments of 200~300 bp on 2% Low Range Ultra Agarose followed by PCR amplified using Phusion DNA polymerase (NEB) for 15 PCR cycles.
|
| |
|
| Library strategy |
ssRNA-seq |
| Library source |
transcriptomic |
| Library selection |
cDNA |
| Instrument model |
Illumina NovaSeq 6000 |
| |
|
| Description |
Gene expression data from Staphylococcus aureus grown till exponential phase
|
| Data processing |
The raw paired end reads were trimmed and quality controlled by Trimmomatic with default parameters.
Then clean reads were separately aligned to reference genome with orientation mode using HISAT.
To identify DEGs (differential expression genes) between two different samples, the expression level for each transcript was calculated using the fragments per kilobase of read per million mapped reads (RPKM) method. The method Bowtie2 and RSEM were used for differential expression analysis
Genome_build: Staphylococcus aureus COL
Supplementary_files_format_and_content: RPKMs, DEGs
|
| |
|
| Submission date |
Jan 04, 2022 |
| Last update date |
Oct 15, 2022 |
| Contact name |
Qing Wei |
| E-mail(s) |
[email protected]
|
| Organization name |
Institute of Microbiology, Chinese Academy of Sciences
|
| Lab |
Biofilm Research Group
|
| Street address |
NO.1 Beichen West Road, Chaoyang District
|
| City |
Beijing |
| ZIP/Postal code |
100101 |
| Country |
China |
| |
|
| Platform ID |
GPL27158 |
| Series (1) |
| GSE193011 |
Transcriptional responses of CDCA treated Staphylococcus aureus cells |
|
| Relations |
| BioSample |
SAMN24608348 |
| SRA |
SRX13597241 |
