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Sample GSM855600 Query DataSets for GSM855600
Status Public on Mar 05, 2013
Title Mock roots-0dpi-biological rep2
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 685.5773064
AFFX-BioB-5_at 695.4638284
AFFX-BioB-M_at 734.5068039
AFFX-BioC-3_at 948.1891829
AFFX-BioC-5_at 1200.881028
AFFX-BioDn-3_at 5171.47667
AFFX-BioDn-5_at 1752.125625
AFFX-CreX-3_at 18676.8664
AFFX-CreX-5_at 16419.05107
AFFX-DapX-3_at 27949.66987
AFFX-DapX-5_at 10696.58548
AFFX-DapX-M_at 24694.35301
AFFX-LysX-3_at 9568.740922
AFFX-LysX-5_at 3389.1213
AFFX-LysX-M_at 5075.046984
AFFX-Msa-16SrRNA_s_at 140.7243507
AFFX-Msa-26SrRNA_at 20.73848047
AFFX-Msa-5SrRNA_s_at 143.9784188
AFFX-Msa-actin-3_at 1759.905767
AFFX-Msa-actin-5_at 131.6440565

Total number of rows: 969

Table truncated, full table size 27 Kbytes.




Supplementary file Size Download File type/resource
GSM855600_0dmr_2.CEL.gz 139.8 Kb (ftp)(http) CEL
Processed data included within Sample table

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