NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2218739 Query DataSets for GSM2218739
Status Public on Dec 31, 2018
Title T24_3
Sample type SRA
 
Source name T24 leaves
Organism Andrographis paniculata
Characteristics tissue: leaf
induction stage: T24
Extracted molecule total RNA
Extraction protocol Total RNAs from leaves induced for 0, 12, 24 and 48 hours with three biological replicates were extracted using Trizol (Invitrogen, 15596-018) according to the manufacturer’s instructions. Highly purified and intact mRNAs were enriched from total RNAs using Dynabeads® mRNA purification kit (Ambion, 61006). RNAs were fragmented into ~ 300 nt fragments by 1 min incubation at 94℃ in fragmentation buffer (10 mM ZnCl2, 10 mM Tris-HCl, pH 7.0). The fragmentation reaction was stopped with 50 mM EDTA, followed by standard ethanol precipitation and collected for sequencing and expression validation.
For the strand-specific RNA-seq, fragmented RNAs were re-suspended in H2O and used for library generation with mRNA sequencing kit (Illumina Inc. San Diego, CA). Sequencing was carried out on Illumina HiSeq 4000 sequencer (Illumina Inc. San Diego, CA) according to the manufacturer’s instructions and 150 nt paired-end sequencing reads were generated.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 4000
 
Description T24_3
MeJA induce for 24 hours
Data processing Base-calling were performed using RTA and CASAVA.
The quality of sequencing data was estimated using FastQC (v0.11.3). Then adaptors and low quality bases were removed using Trimmomatic (v0.33).
Clean reads from all samples were pooled together and feeded to de novo RNA-seq assembly software Trinity (v2.0.6) with default parameters.
The expression of assembled transcripts and genes were quantified using RSEM (v1.2.19).
Genome_build: n/a
Supplementary_files_format_and_content: Tab-delimited text files include FPKM values of each transcript for all samples.
 
Submission date Jun 27, 2016
Last update date May 15, 2019
Contact name Tong Chen
E-mail(s) chentong_biology@163.com
Phone 86-15210822685
Organization name China Academy of Chinese Medical Sciences
Department State Key Laboratory Breeding Base of Dao-di Herbs, National Resource Center for Chinese Materia Medica
Lab Luqi Huang's lab
Street address No 16 Nan-xiao-jie Dong-zhi-men-nei
City Beijing
ZIP/Postal code 100700
Country China
 
Platform ID GPL22087
Series (1)
GSE83775 Time-serialized expression profile of MeJA induced Andrographis paniculata leaves
Relations
BioSample SAMN05296545
SRA SRX1880254

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap