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Sample GSM855626 Query DataSets for GSM855626
Status Public on Mar 05, 2013
Title Sm1021 innoculated roots-7dpi-biological rep1
Sample type RNA
 
Source name Medicago truncatula roots were innoculated with Sm1021 WT rhizobia, and nodulated roots were harvested after 7 days
Organism Medicago truncatula
Characteristics plant age: 12 days
treatment: inoculated with Sinorhizobium meliloti Sm1021
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 innoculated with Sm1021 WT rhizobia
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 905.2066599
AFFX-BioB-5_at 844.018271
AFFX-BioB-M_at 872.8578099
AFFX-BioC-3_at 1184.363864
AFFX-BioC-5_at 1421.944972
AFFX-BioDn-3_at 7807.016804
AFFX-BioDn-5_at 2590.538806
AFFX-CreX-3_at 24556.81962
AFFX-CreX-5_at 20840.95606
AFFX-DapX-3_at 4013.759017
AFFX-DapX-5_at 1525.706427
AFFX-DapX-M_at 3122.877685
AFFX-LysX-3_at 551.2523307
AFFX-LysX-5_at 200.9229533
AFFX-LysX-M_at 241.4997661
AFFX-Msa-16SrRNA_s_at 75.41900405
AFFX-Msa-26SrRNA_at 52.8237419
AFFX-Msa-5SrRNA_s_at 113.6420561
AFFX-Msa-actin-3_at 1022.511452
AFFX-Msa-actin-5_at 96.03615804

Total number of rows: 969

Table truncated, full table size 27 Kbytes.




Supplementary file Size Download File type/resource
GSM855626_sm7d_1.CEL.gz 139.1 Kb (ftp)(http) CEL
Processed data included within Sample table

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