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Sample GSM293195 Query DataSets for GSM293195
Status Public on May 30, 2008
Title 77_1130.1O.R082P, Experimental replicate 1
Sample type RNA
Source name Soybean cultivar RIL 082 - RNA taken from entire inoculated area inoculated with water + agar(mock sample): Timepoint: NA
Organism Glycine max
Characteristics cultivar - RIL 082
Tissue/Cell Type: Soybean root/hypocotyls - P.sojae mycelium from minimal medium
Treatment protocol Soybean plants were grown in growth chambers and transferred to trays prior to inoculation. There were 3 trays for each treatment type having 10 plants each. P.sojae materials were inoculated onto the roots of the host plant and RNA extraction was carried out either on 3rd day or 5th day post inoculation. For mock inoculation, the plants were inoculated with pure water with agar. For RIL experiments the RILS had no specific time points but the checks did.
Growth protocol Soybean plants were grown in growth chambers and later transferred to trays with clothes soaked in water
Extracted molecule total RNA
Extraction protocol QIAGEN RNeasy Kit : As recommended by manufacturer
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from total RNA. RNA is is first reverse transcribed using a T7-Oligo(dT) Promoter Primer in the first-strand cDNA synthesis reaction. Following RNase H-mediated second-strand cDNA synthesis, the double-stranded cDNA is purified and serves as a template in the subsequent in vitro transcription (IVT) reaction. The IVT reaction is carried out in the presence of T7 RNA Polymerase and a biotinylated nucleotide analog/ribonucleotide mix for complementary RNA (cRNA) amplification and biotin labeling. The biotinylated cRNA targets are then cleaned up, fragmented, and hybridized to GeneChip expression arrays(Affymetrix Technical manual - 2004)
Hybridization protocol hybridization cocktail is prepared, including the fragmented target, probe array controls, BSA, and herring sperm DNA. It is then hybridized to the probe array during a 16-hour incubation(Affymetrix technical manual - 2004)
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneChip Scanner 3000
Description Data was collected from the hypocotyl regions of Soybean plants at different time points
Data processing The data were analyzed with RMA suite from R package version 2.4.0. Background correction was using RMA followed by quantile normalization and data was summarized using median polish method
Submission date May 29, 2008
Last update date May 30, 2008
Contact name sucheta Tripathy
Phone 5402318138
Organization name Virginia Tech
Department Virginia Bioinformatics Institute
Lab Tyler lab
Street address 1, Washington street
City Blacksburg
State/province VA
ZIP/Postal code 24061
Country USA
Platform ID GPL4592
Series (1)
GSE11611 Combined gene expression and QTL analysis of soybean quantitative resistance to Phytophthora sojae

Data table header descriptions
VALUE RMA processed value

Data table
Gma.1.1.A1_at 3.604021
Gma.1.1.S1_at 4.441505
Gma.10.1.S1_at 2.394264
Gma.100.1.A1_at 6.054767
Gma.10004.1.S1_at 8.567114
Gma.10005.1.S1_at 6.613396
Gma.1001.1.A1_at 2.651497
Gma.10013.1.S1_at 7.464701
Gma.10015.1.S1_at 10.747966
Gma.10016.1.S1_at 9.154747
Gma.1002.1.A1_at 2.797701
Gma.1002.2.S1_at 2.165649
Gma.10024.1.S1_at 2.179450
Gma.10026.1.S1_at 6.106286
Gma.10027.1.S1_at 3.608151
Gma.10029.1.S1_at 7.775937
Gma.1003.1.S1_at 8.495084
Gma.10031.1.S1_at 8.971634
Gma.10032.1.S1_at 2.717222
Gma.10033.1.A1_at 2.685311

Total number of rows: 37593

Table truncated, full table size 1080 Kbytes.

Supplementary file Size Download File type/resource
GSM293195.CEL.gz 5.1 Mb (ftp)(http) CEL
Processed data included within Sample table
Raw data provided as supplementary file

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