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Sample GSM2253800 Query DataSets for GSM2253800
Status Public on Jul 28, 2016
Title Root_1
Sample type RNA
 
Source name Root at 14 days
Organism Oryza sativa
Characteristics self-fertile and virulent on host plants: Oryza sativa L. cv. Dongjin
cultivar: Oryza sativa L. cv. Dongjin
Treatment protocol The calli were induced from seeds on 2N6 medium at 37°C for 4 weeks. The regenerating calli were induced from calli for 2 weeks on a MS16 medium and collected when turned green. The seeds were germinated on water-soaked filter paper for 4 days in a dark chamber. Leaves and roots were harvested separately 14 days after sowing in soil. A flower sample was harvested at exact stages following recommendations from previous research. The flowers before pollination were prepared just prior to the opening of the spikelet, and the flowers after pollination were collected followed by anthesis, respectively. The flower before pollination (FBP) was collected prior to the opening of the spikelet, and its pistil length was in the range of 0.5 to 1.5 mm. The flower after pollination (FAP) was collected after the anthesis and maximum opening of the florets.
Growth protocol All seven tissues in this study were prepared from Oryza sativa L. cv. Dongjin.
Extracted molecule total RNA
Extraction protocol Total RNAs were extracted using TriReagent (Molecular Research Center, Inc.).
Label Cy3
Label protocol Labeling was performed by NimbleGen Systems Inc., Madison, WI USA, following their standard operating protocol. See www.nimblegen.com.
 
Hybridization protocol Hybridization was performed by NimbleGen Systems Inc., Madison, WI, USA following their standard operating protocol. See www.nimblegen.com.
Scan protocol Scanning was performed by NimbleGen Systems Inc., Madison, WI USA, following their standard operating protocol. See www.nimblegen.com.
Description Roots were harvested separately 14 days after sowing in soil.
Data processing The raw data (.pair file) was subjected to RMA (Robust Multi-Array Analysis; Irizarry et al. Biostatistics 4(2):249), quantile normalization (Bolstad et al. Bioinformatics 19(2):185), and background correction as implemented in the NimbleScan software package, version 2.4.27 (Roche NimbleGen, Inc.).
 
Submission date Jul 27, 2016
Last update date Jul 28, 2016
Contact name Yeon-Ki Kim
E-mail(s) kim750a11@gmail.com
Phone 82-31-321-6351
Organization name GreenGene Biotech Inc.
Department GreenGene Biotech Inc.
Lab Genomics & Genetics Ins.
Street address 38-2 Namdong
City Yongin
State/province Kyonggido
ZIP/Postal code 449-728
Country South Korea
 
Platform ID GPL22243
Series (1)
GSE84903 Analysis of representative organ specific genes and promoters of rice using 3’ ORF oriented long oligomer microarray

Data table header descriptions
ID_REF
VALUE RMA-normalized, averaged gene-level signal intensity

Data table
ID_REF VALUE
AK105202 12952.6
AB001883 1272.53
AB001885 1300.02
AB001887 893.058
AB001888 4215.46
AB002266 3146
AB003496 5138.29
AK103345 4420.84
AB004799 3257.84
AB005620 4816.84
AB007193 2990.6
AB007194 2310.3
AB007405 19814.1
AB007501 13587.3
AB007623 1323.95
AB008519 999.735
AB008845 19294.1
AB010740 27274.5
AB011271 22088
AB015288 16794.4

Total number of rows: 26257

Table truncated, full table size 455 Kbytes.




Supplementary file Size Download File type/resource
GSM2253800_Root_1_040507_532.probe.gz 6.1 Mb (ftp)(http) PROBE
GSM2253800_Root_1_532_nm_norm_RMA.pair.gz 6.4 Mb (ftp)(http) PAIR
Processed data included within Sample table
Processed data provided as supplementary file

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