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Sample GSM3231398 Query DataSets for GSM3231398
Status Public on Jul 04, 2018
Title CP_ZnF8_control_r3
Sample type SRA
 
Source name Tiller bases
Organism Oryza sativa Japonica Group
Characteristics experiment objectives: analysis of differentially expressed genes
tissue: Tiller bases
development stage: Tillering stage
genotype: control plants of ZnF8 transgenic lines
phenotype: erect growth
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using TRIzol according to the instructions.
P-aired-end libraries were constructed using a TruSeq RNA Sample Preparation Kit v2.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Data processing Raw reads were mapped to the reference genome by TopHat using default parameters.
Cuffdiff was used to calculate the FPKM (fragments per kilobase of exon per million mapped reads) of each gene and to identify the differentially-expressed genes (fold change ≥ 2, P < 0.001) between the CP-PROG1, CP-ZnF5, CP-ZnF7, CP-ZnF8 and control plants.
The functional category analysis of the differentially-expressed genes was performed by the AgriGO and KEGG databases.
Genome_build: Os-Nipponbare-Reference-IRGSP-1.0, MSU7
 
Submission date Jun 28, 2018
Last update date Jul 04, 2018
Contact name Ma Xin
Organization name China Agricultural University
Street address 2 Yuanmingyuan West Road, Haidian District, Beijing, China, 2 Yuanmingyuan West Road, Haidian District, Beijing, China
City Beijing
State/province --- Select a state ---
ZIP/Postal code 100193
Country China
 
Platform ID GPL18525
Series (1)
GSE116423 Chromosomal deletions drove parallel domestication of plant architecture in Asian and African rice
Relations
BioSample SAMN09516007
SRA SRX4321427

Supplementary file Size Download File type/resource
GSM3231398_CP_ZnF8_r3.fpkm.txt.gz 267.6 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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