NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM238032 Query DataSets for GSM238032
Status Public on Apr 15, 2008
Title Soybean-2601R-4-RMA
Sample type RNA
 
Source name Soybean strain 2601R
Organism Glycine max
Characteristics Strain: 2601R
Growth Stage: V2
Biomaterial provider First Line Seeds Ltd., Guelph, ON, Canada
Growth protocol Grown in growth changers in ambient humidity, 16h photoperiod, and 25/19°C day/night temperatures. 10 seeds sown into two 20 cm pots.
Extracted molecule total RNA
Extraction protocol At the V2 growth stage (Fehr et al. 1971), completely unrolled first trifoliate leaves were harvested by cutting the petiole a few millimeters below the leaflets, immediately frozen in liquid nitrogen and stored at -80°C. RNA was extracted using the RNeasy Plant Mini Kit (Quiagen, Valencia, CA).
Label biotin
Label protocol 5µg of total RNA was used to generate double-stranded cDNA using a T7-linked oligo(dT) primer and SuperScript II reverse transcriptase (Invitrogen) following the instructions for the One cycle-cDNA synthesis kit (from Affymetrix). cRNA were synthesized using the IVT labelling kit from Affymetrix, resulting in biotinylated cRNA.
 
Hybridization protocol Target preparation, hybridization and scanning were carried out at the McGill University and Genome Quebec Innovation Centre Microarray platform using the protocol recommended by Affymetrix (). Labelled cRNA were cleaned and fragmented using the Sample Cleanup Module reagents (Qiagen). Spike controls B2, bio-B, bio-C, bio-D, and Cre-x were added to the hybridization cocktail before overnight hybridization at 45°C for 16 h.
Scan protocol Arrays were washed and stained in an Affymetrix fluidics Station prior to scanning on the GeneChip Scanner 3000 (Affymetrix). Image acquisition and processing was done with the Microarray Analysis Suite 5.0 (Affymetrix).
Description Sample 4 from the 2601R soybean strain. The third of five samples for this strain.
Data processing R and the BioConductor packages (Gentleman et al., 2004) such as affy, limma, cluster, and made4 were used for data analysis. This sample was pre-processed using the RMA method.
 
Submission date Oct 17, 2007
Last update date Aug 14, 2011
Contact name Martina Stromvik
E-mail(s) [email protected]
Phone +1 (514) 398 8627
Fax +1 (514) 398 7897
URL http://www.mcgill.ca/plant/faculty/stromvik/
Organization name McGill University
Department Department of Plant Science
Lab Plant Bioinformatics
Street address 21,111 Lakeshore Rd
City Ste-Anne-de-Bellevue
State/province Quebec
ZIP/Postal code H9X 3V9
Country Canada
 
Platform ID GPL4592
Series (1)
GSE9374 Exploration of microarrays as tools to assess substantial equivalence of genetically modified soybeans

Data table header descriptions
ID_REF
VALUE RMA normalized probe intensities
SCALE log scale for RMA pre-processed data

Data table
ID_REF VALUE SCALE
AFFX-BioB-3_at 6.87005661063865 log2
AFFX-BioB-5_at 7.41906306944498 log2
AFFX-BioB-M_at 7.53943067334698 log2
AFFX-BioC-3_at 8.869642991893 log2
AFFX-BioC-5_at 8.3590817682573 log2
AFFX-BioDn-3_at 11.1261569609174 log2
AFFX-BioDn-5_at 10.1576716723841 log2
AFFX-CreX-3_at 12.4319666632729 log2
AFFX-CreX-5_at 11.8818222187238 log2
AFFX-DapX-3_at 8.99959318914554 log2
AFFX-DapX-5_at 7.16920339690474 log2
AFFX-DapX-M_at 8.12338986914813 log2
AFFX-Gm_18SrRNA_at 4.55276661968802 log2
AFFX-Gm_Actin_3_at 8.4651918413022 log2
AFFX-Gm_Actin_5_at 1.51013687458874 log2
AFFX-Gm_Actin_M_at 5.20147546191965 log2
AFFX-Gm_GlutTrans_3_r_at 10.4366499654208 log2
AFFX-Gm_GlutTrans_5_s_at 8.02291224856127 log2
AFFX-Gm_GlutTrans_M_at 9.51569053926788 log2
AFFX-Gm_P450_3_s_at 5.74890649514015 log2

Total number of rows: 61170

Table truncated, full table size 2538 Kbytes.




Supplementary file Size Download File type/resource
GSM238032.CEL.gz 7.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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