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Series GSE52596 Query DataSets for GSE52596
Status Public on Jun 20, 2014
Title EXPRSS: an Illumina based high-throughput expression-profiling method to reveal transcriptional dynamics - III
Organism Arabidopsis thaliana
Experiment type Expression profiling by high throughput sequencing
Summary Background
Next Generation Sequencing technologies have facilitated differential gene expression analysis through RNA-seq and Tag-seq methods. RNA-seq has biases associated with transcript lengths, lacks uniform coverage of regions in mRNA and requires 10–20 times more reads than a typical Tag-seq. Most existing Tag-seq methods either have biases or not high throughput due to use of restriction enzymes or enzymatic manipulation of 5’ ends of mRNA or use of RNA ligations.

Results
We have developed EXpression Profiling through Randomly Sheared cDNA tag Sequencing (EXPRSS) that employs acoustic waves to randomly shear cDNA and generate sequence tags at a relatively defined position (~150-200 bp) from the 3′ end of each mRNA. Implementation of the method was verified through comparative analysis of expression data generated from EXPRSS, NlaIII-DGE and Affymetrix microarray and through qPCR quantification of selected genes. EXPRSS is a strand specific and restriction enzyme independent tag sequencing method that does not require cDNA length-based data transformations. EXPRSS is highly reproducible, is high-throughput and it also reveals alternative polyadenylation and polyadenylated antisense transcripts. It is cost-effective using barcoded multiplexing, avoids the biases of existing SAGE and derivative methods and can reveal polyadenylation position from paired-end sequencing.

Conclusions
EXPRSS Tag-seq provides sensitive and reliable gene expression data and enables high-throughput expression profiling with relatively simple downstream analysis.

 
Overall design Four-week-old Arabidopsis (No-0 and slh1) plants were grown at 28°C and transferred to a 21°C growth chamber. Time course samples were collected after the temperature shift; mRNA profiles were generated by deep sequencing on Illumina MiSeq using EXPRSS protocol.
 
Contributor(s) Rallapalli G, Kemen EM, MacLean D, Robert-Seilaniantz A, Segonzac C, Etherington G, Sohn KH, Jones JD
Citation(s) 24884414
Submission date Nov 20, 2013
Last update date May 15, 2019
Contact name Ghanasyam Rallapalli
E-mail(s) g.rallapalli@uea.ac.uk
Organization name The Sainsbury Laboratory
Street address Norwich Research Park
City Norwich
ZIP/Postal code NR4 7UH
Country United Kingdom
 
Platforms (1)
GPL17970 Illumina MiSeq (Arabidopsis thaliana)
Samples (9)
GSM1272330 No-0_00hr
GSM1272331 No-0_06hr
GSM1272332 No-0_09hr
This SubSeries is part of SuperSeries:
GSE51721 EXPRSS: an Illumina based high-throughput expression-profiling method to reveal transcriptional dynamics
Relations
BioProject PRJNA229430
SRA SRP033221

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE52596_RAW.tar 660.0 Kb (http)(custom) TAR (of TXT)
GSE52596_barcode_info.txt.gz 201 b (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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