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Sample GSM357667 Query DataSets for GSM357667
Status Public on Nov 11, 2010
Title Regenerating callus 2 days, biological rep1
Sample type RNA
 
Source name 2 days regenerated callus
Organism Oryza sativa
Characteristics cv. Nipponbare
Treatment protocol Collected biological samples were frozen in liquid nitrogen and kept -80C until RNA extraction.
Growth protocol Young leaves and roots were collected from plants grown in a green house. Calli were generated from seeds for three weeks on MS medium at 30C, transferred to regeration medium, cultured for indicated days and collected. Shoots were collected from plants grown at 30C in a growth chamber for four weeks.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted with RNeasy plant mini kit (Qiagen) according to manufacturer's protocol.
Label biotin
Label protocol Biotinylated cRNA were prepared from 500 ng total RNA using One-Cycle cDNA Synthesis Kit (Affymetrix) according to manufacturers protocol (hws_kit_manual).
 
Hybridization protocol 3.3 ug of labeled and fragmented cRNA was hybridized to GeneChip Rice Genome Array using GeneChip Hybridization Oven 640 (Affymetrix). Wash and stain was performed by GeneChip Fluidics Station 450 (Affymetrix). All operations were performed with Hybridization, Stain and Wash Kit (Affymetrix) according to manufacturer's protocol (hws_kit_manual).
Scan protocol GeneChips were scanned using GeneChip Scanner 3000 7G (Affymetrix).
Description Gene expression data from regenerating callus.
Data processing CEL files produced by GCOS 1.3 were analyzed using the statistical software R with bioconductor package “affy”. Signal intensities were extracted by expresso algorithm with parameters : bgcorrect.method = “mas”, normalize = “F”, pmcorrect.method = “pmonly”, summary.method = “mas”. Extracted signal intensities were introduced into GeneSpring 7.3.1 (Agilent) and scaled to 75th percentile per chip. Mas5calls algorithm in package “affy” was used for detection call.
 
Submission date Jan 06, 2009
Last update date Nov 11, 2010
Contact name Nori Kurata
E-mail(s) nkurata@nig.ac.jp
Phone +81-55-981-6808
Organization name National Institute of Genetics
Lab Plant genetics Lab.
Street address 1111 Yata
City Mishima
State/province Shizuoka
ZIP/Postal code 411-8540
Country Japan
 
Platform ID GPL2025
Series (2)
GSE14300 Rice expression atlas (4): Vegetative tissues
GSE14304 Rice expression atlas: Plant reproductive process

Data table header descriptions
ID_REF
VALUE Normalized signal intensity
ABS_CALL

Data table
ID_REF VALUE ABS_CALL
AFFX-BioB-3_at 2.2119536 P
AFFX-BioB-5_at 2.312942 P
AFFX-BioB-M_at 2.7433255 P
AFFX-BioC-3_at 6.452906 P
AFFX-BioC-5_at 5.8435516 P
AFFX-BioDn-3_at 32.511917 P
AFFX-BioDn-5_at 14.631019 P
AFFX-CreX-3_at 107.35026 P
AFFX-CreX-5_at 79.033 P
AFFX-DapX-3_at 1.2470515 P
AFFX-DapX-5_at 0.24700512 P
AFFX-DapX-M_at 0.5465421 P
AFFX-LysX-3_at 0.3665146 P
AFFX-LysX-5_at 0.12229582 P
AFFX-LysX-M_at 0.20319536 A
AFFX-Mgr-actin-3_at 0.17867497 A
AFFX-Mgr-actin-5_at 0.18383032 A
AFFX-Mgr-actin-M_at 0.29046884 A
AFFX-Mgr-ef1a-3_at 0.35875002 A
AFFX-Mgr-ef1a-3_x_at 0.31374353 A

Total number of rows: 57381

Table truncated, full table size 1764 Kbytes.




Supplementary file Size Download File type/resource
GSM357667.CEL.gz 4.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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