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Sample GSM855607 Query DataSets for GSM855607
Status Public on Mar 05, 2013
Title Mock roots-7dpi-biological rep3
Sample type RNA
 
Source name Medicago truncatula roots were treated with sterile water and harvested from mock innoculated plants after 7 days.
Organism Medicago truncatula
Characteristics plant age: 12 days
treatment: mock inoculated
treatment-time: 7 days
tissue: roots
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 10 ug total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on to the AtMtDEFL custom Array. GeneChips were washed and stained using the MAUI 12-bay hybridization system.
Scan protocol GeneChips were scanned using the MAUI 12-bay hybridization system.
Description Gene expression data from 7 dpi root segments excluding the root tip of plants mock innoculated with sterile water and used as control for Sinorhizobium meliloti Sm1021 innoculated roots.
Data processing Microarray normalizations and initial analyses were performed in R using custom scripts that made use of Bioconductor routines. To implement the Stable-genes Based Quantile (SBQ) normalization (Sato et al., 2007), we first combined expression data from all 11 probes within a probe set into a single expression measure using the Bioconductor expression command, using RMA-style background correction and median polish probe summarization. These summarized values were output from R and used as input to the SBQ perl script (Sato et al., 2007).For statistical analysis, SBQ normalized signal intensity values were Log2 transformed and statistical analysis was based on a t-test or ANOVA (P<0.05) with Benjamini and Hochberg false discovery rate multiple testing correction (Benjamini and Hochberg, 1995), and the corrected p values were designated as q values.
 
Submission date Jan 03, 2012
Last update date Mar 06, 2013
Contact name Kevin A Silverstein
Organization name Universtiy of Minnesota
Department Minnesota Supercomuting Institute
Street address 599 Walter Library, 117 Pleasant St SE
City Minneapolis
State/province MN
ZIP/Postal code 55455
Country USA
 
Platform ID GPL14988
Series (1)
GSE34803 Expression data of Nodule Cysteine-Rich (NCR) Defensin-Like (DEFL) genes in different stages of nodule development in Medicago truncatula

Data table header descriptions
ID_REF
VALUE SBQ normalized signal intensity values

Data table
ID_REF VALUE
AFFX-BioB-3_at 742.0339751
AFFX-BioB-5_at 727.1472736
AFFX-BioB-M_at 750.1134396
AFFX-BioC-3_at 1138.220522
AFFX-BioC-5_at 1258.654377
AFFX-BioDn-3_at 7008.982545
AFFX-BioDn-5_at 1961.671772
AFFX-CreX-3_at 18035.37844
AFFX-CreX-5_at 16276.47017
AFFX-DapX-3_at 26066.79004
AFFX-DapX-5_at 4325.46205
AFFX-DapX-M_at 17173.40518
AFFX-LysX-3_at 10063.95848
AFFX-LysX-5_at 2806.403062
AFFX-LysX-M_at 5925.917196
AFFX-Msa-16SrRNA_s_at 430.2075942
AFFX-Msa-26SrRNA_at 17.89523453
AFFX-Msa-5SrRNA_s_at 266.0050195
AFFX-Msa-actin-3_at 550.3837762
AFFX-Msa-actin-5_at 151.5168356

Total number of rows: 969

Table truncated, full table size 27 Kbytes.




Supplementary file Size Download File type/resource
GSM855607_7dmr_3.CEL.gz 139.5 Kb (ftp)(http) CEL
Processed data included within Sample table

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