|
Status |
Public on Feb 14, 2024 |
Title |
KO_R.DraR1,no_stress,rep1 |
Sample type |
SRA |
|
|
Source name |
cells
|
Organism |
Deinococcus radiodurans |
Characteristics |
tissue: cells genotype: KO_R.DraR1-1
|
Growth protocol |
tryptone glucose yeast extract (TGY) liquid media at 30◦C
|
Extracted molecule |
total RNA |
Extraction protocol |
Total RNA was isolated using the Trizol method.1% denaturing agarose gels were used to assess RNA degradation and contamination. RNA concentration and RNA integrity were measured using an RNA Nano 6000 Assay kit and Bioanalyzer 2100 system. A total of 3G RNA text per sample was used as the input material for library preparation.
|
|
|
Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina NovaSeq 6000 |
|
|
Data processing |
The library preparations were sequenced on an Illumina Hiseq platform and paired-end reads were generated. Assembly: Deinococcus radiodurans R1 Supplementary files format and content: table delimited text files include FPKM values for each sample
|
|
|
Submission date |
Dec 20, 2023 |
Last update date |
Feb 14, 2024 |
Contact name |
Chenxiang Shi |
E-mail(s) |
[email protected]
|
Organization name |
Zhejiang University
|
Street address |
Sandun Zhen Yuhangtang Road 866
|
City |
Hangzhou |
State/province |
Zhejiang province |
ZIP/Postal code |
1 |
Country |
China |
|
|
Platform ID |
GPL31018 |
Series (1) |
GSE251690 |
Characterization of a novel N4 -methylcytosine restriction-modification system in Deinococcus radiodurans |
|
Relations |
SRA |
SRX22919957 |
BioSample |
SAMN38879806 |