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Sample GSM7986056 Query DataSets for GSM7986056
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

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA

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