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Sample GSM855613 Query DataSets for GSM855613
Status Public on Mar 05, 2013
Title Mock roots-40dpi-biological rep3
Sample type RNA
 
Source name Medicago truncatula roots were treated with sterile water and harvested from mock innoculated plants after 40 days.
Organism Medicago truncatula
Characteristics plant age: 45 days
treatment: mock inoculated
treatment-time: 40 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 40 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 1034.108203
AFFX-BioB-5_at 1105.438819
AFFX-BioB-M_at 1029.768361
AFFX-BioC-3_at 1625.328715
AFFX-BioC-5_at 2060.908313
AFFX-BioDn-3_at 8278.149323
AFFX-BioDn-5_at 2603.43233
AFFX-CreX-3_at 19886.35476
AFFX-CreX-5_at 17788.08504
AFFX-DapX-3_at 17556.43863
AFFX-DapX-5_at 7282.144545
AFFX-DapX-M_at 12263.79649
AFFX-LysX-3_at 4980.05482
AFFX-LysX-5_at 2392.753794
AFFX-LysX-M_at 2859.188593
AFFX-Msa-16SrRNA_s_at 181.7503244
AFFX-Msa-26SrRNA_at 40.52532546
AFFX-Msa-5SrRNA_s_at 326.2635828
AFFX-Msa-actin-3_at 1142.756303
AFFX-Msa-actin-5_at 147.9466606

Total number of rows: 969

Table truncated, full table size 27 Kbytes.




Supplementary file Size Download File type/resource
GSM855613_m40_4.CEL.gz 137.2 Kb (ftp)(http) CEL
Processed data included within Sample table

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