NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1017171 Query DataSets for GSM1017171
Status Public on Oct 22, 2012
Title PTB_OE2_R1
Sample type SRA
 
Source name seedlings
Organism Arabidopsis thaliana
Characteristics ecotype: Columbia
genotype: At5g53180 overexpression
developmental stage: 11 days old seedlings
Growth protocol Arabidopsis seeds were surface sterilized and plated on 1/2 MS medium containing 2% sucrose and 0.8% phytoagar. Following stratification for 2 days in darkness at 4°C plates were transferred to continuous light (~20°C, ~60% humidity). Seedlings were sampled after cultivation for 11 days.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from ∼100 mg of plant tissue using the Universal RNA Purification kit (EURx), including an on-column DNaseI treatment performed according to the manufacturer's instructions.
Libraries were prepared using the Illumina TruseqTM sample prep kit (Illumina) according to the manufacturer's instructions (TruSeqTM RNA Sample Preparation v2 Guide, version: November 2010). For the adapter ligation step, the RNA Adapter Indexes 10 (AR010) and 13 (AR013) were used. Following the PCR enrichment step using half the sample volume, libraries were subjected to an additional gel purification step. A size range of 250-350 bp was extracted from a 2% agarose gel and purified using the MinElute Gel Extraction Kit (Qiagen).
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina Genome Analyzer II
 
Description 429 R1 (oe_2)
Data processing Illumina Raw Data processing with SHORE 4.1 pipeline with application 'mRNA' and disabled Illumina filter
fastq files were aligned to the TAIR10 reference genome with the spliced aligner PALMapper (version 4)
Alignment postprocessing (filtering and multimapper resolution) using RNAgeeq
Reads were counted as overlapping to a gene, if they shared at least one exonic position
Expression values were transformed to RPKM (Reads per kilobase per million mapped reads)
Genome_build: TAIR10
Supplementary_files_format_and_content: Tab delimited text-file, with following columns: (1) gene id; (2) WT; (3) MI12; (4) MI3; (5) OE1; (6) OE2; (7) OE3
 
Submission date Oct 09, 2012
Last update date May 15, 2019
Contact name Andre Kahles
E-mail(s) akahles@cbio.mskcc.org
Organization name Memorial Sloan-Kettering Cancer Center
Department Computational Biology Center
Lab Rätsch Lab
Street address 1275 York Avenue
City New York
State/province New York
ZIP/Postal code 10065
Country USA
 
Platform ID GPL9302
Series (1)
GSE41433 Polypyrimidine tract-binding protein homologues from Arabidopsis are key regulators of alternative splicing with implications in fundamental developmental processes
Relations
SRA SRX193195
BioSample SAMN01760500

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