|
Status |
Public on Oct 17, 2022 |
Title |
TPA·2Na |
Sample type |
SRA |
|
|
Source name |
bacterial cell
|
Organism |
Piscinibacter sakaiensis |
Characteristics |
strain: 201-F6 cell type: bacterial cell genotype: wild-type time: 20 h
|
Growth protocol |
Cells were cultured in a test tube containing YSV medium with a PET film, TPA·2Na, or EG as the primary carbon source for 20 h.
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was extracted and purified using the RNeasy Mini Kit (Qiagen) with on-column DNA digestion using RNase-Free DNase Set (Qiagen). Bacterial 16S and 23S ribosomal RNAs were removed from total RNA with the Ribo-Zero rRNA removal kit for gram-negative bacteria (Illumina, San Diego, CA). The enriched mRNA fraction was converted to an RNA-Seq library with multiplexing adaptors.
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
BGISEQ-500 |
|
|
Data processing |
CLC Genomics Workbench v 20.0 Sequence reads were trimmed for adaptor sequence/low-quality sequence Trimmed sequence reads were mapped to ASM129352v1 using CLC genomic workbench (parameters- mismath cost: 2 insertion cost: 3 deletion cost: 3 length fraction: 0.8 similarity fraction: 0.8) Read count extraction and normalization were performed using CLC genomic benchwork Assembly: ASM129352v1 Supplementary files format and content: tab-delimited text files include RPKM values for each Sample
|
|
|
Submission date |
Jun 10, 2022 |
Last update date |
Oct 17, 2022 |
Contact name |
Shosuke Yoshida |
E-mail(s) |
ssk-yoshida@bs.naist.jp
|
Organization name |
Nara Institute of Science and Technology
|
Street address |
8916-5 Takayama-cho
|
City |
Ikoma |
State/province |
Nara |
ZIP/Postal code |
630-0192 |
Country |
Japan |
|
|
Platform ID |
GPL32339 |
Series (1) |
GSE205843 |
RNA-seq of Ideonella sakaiensis 201-F6 when grown on PET, TPA·2Na, and EG |
|
Relations |
BioSample |
SAMN28963196 |
SRA |
SRX15670307 |