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Sample GSM855599 Query DataSets for GSM855599
Status Public on Mar 05, 2013
Title Mock roots-0dpi-biological rep1
Sample type RNA
 
Source name Medicago truncatula roots were treated with sterile water and harvested from mock innoculated plants after 0 days.
Organism Medicago truncatula
Characteristics plant age: 5 days
treatment: mock inoculated
treatment-time: 0 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 0 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 584.6009896
AFFX-BioB-5_at 559.7730289
AFFX-BioB-M_at 585.7716205
AFFX-BioC-3_at 868.7112475
AFFX-BioC-5_at 954.6099077
AFFX-BioDn-3_at 4225.934193
AFFX-BioDn-5_at 1623.172409
AFFX-CreX-3_at 17101.42158
AFFX-CreX-5_at 14663.26937
AFFX-DapX-3_at 30689.16332
AFFX-DapX-5_at 15149.50931
AFFX-DapX-M_at 27772.62097
AFFX-LysX-3_at 8768.452542
AFFX-LysX-5_at 3927.245124
AFFX-LysX-M_at 5291.913148
AFFX-Msa-16SrRNA_s_at 56.2316447
AFFX-Msa-26SrRNA_at 69.96378002
AFFX-Msa-5SrRNA_s_at 99.30966648
AFFX-Msa-actin-3_at 2612.92597
AFFX-Msa-actin-5_at 147.0351054

Total number of rows: 969

Table truncated, full table size 27 Kbytes.




Supplementary file Size Download File type/resource
GSM855599_0dmr_1.CEL.gz 147.1 Kb (ftp)(http) CEL
Processed data included within Sample table

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