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Sample GSM340569 Query DataSets for GSM340569
Status Public on May 06, 2010
Title Surrounding BS085
Sample type RNA
 
Source name Bladder mucosae surrounding cancer
Organism Homo sapiens
Characteristics biological source: bladder mucosae surrounding cancer
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from tissues with TRIzol (Life Technologies, NY) reagent according to the manufacturer’s protocol. RNA quality and integrity were confirmed by electrophoresis on agarose gel stained with ethidium bromide and examined under ultraviolet light.
Label biotin
Label protocol Biotin-labeled cRNA samples for hybridization were prepared according to Illumina’s recommended sample labeling procedure: 500 ng of total RNA was used for cDNA synthesis, followed by an amplification/labeling step (in vitro transcription) to synthesize biotin-labeled cRNA using the Illumina® TotalPrep RNA Amplification kit (Ambion Inc., Austin, TX). cRNA concentrations using RiboGreen were measured (Quant-iTTM RiboGreen® RNA assay kit; Invitrogen-Molecular Probes, ON, Canada) by the Victor3 spectrophotometer (PerkinElmer, CT) and cRNA quality was checked on a 1% agarose gel.
 
Hybridization protocol Labeled, amplified material (1,500 ng per array) was hybridized to a ver. 2 of the Illumina Human-6 BeadChip (48K) according to the Manufacturer's instructions (Illumina, Inc., San Diego, CA). Array signals were developed by Amersham fluorolink streptavidin-Cy3 (GE Healthcare Bio-Sciences, Little Chalfont, UK) following the BeadChip manual.
Scan protocol Arrays were scanned with an Illumina Bead array Reader confocal scanner (BeadStation 500GXDW; Illumina, Inc., San Diego, CA) according to the Manufacturer's instructions.
Description To export to gene expression data based on unique gene, we use Sample Gene Profile option of Illumina BeadStudio software. Therefore, a total of 5553 probe data which have duplicated gene aggregated unique genes from the whole 48701 probes on the Human-6 beadChip ver. 2.
Data processing Array data processing were performed on Illumina BeadStudio software. We normalized gene expression data using Quantile normalization and log2 transformatoin. To export to a data matrix, Sample Gene Profile option of this software was used.
 
Submission date Nov 07, 2008
Last update date May 06, 2010
Contact name Seon-Kyu Kim
E-mail(s) [email protected]
Phone +82-42-879-8107
Organization name Korea Research Institutue of Bioscience & Biotechnology
Department Personalized Genomic Medicine Research Center
Street address 125 Gwahak-ro, Yuseong-gu, Daejeon 305-806, Korea
City Daejeon
ZIP/Postal code 305-806
Country South Korea
 
Platform ID GPL6102
Series (1)
GSE13507 Predective Value of Prognosis-Related Gene Expression Study in Primary Bladder Cancer

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
ILMN_1725528 9.21
ILMN_1683555 6.91
ILMN_1818771 7.2
ILMN_1773680 7.36
ILMN_1731647 7.69
ILMN_1845201 6.96
ILMN_1746533 8.17
ILMN_1800540 12.81
ILMN_1881186 6.99
ILMN_1878595 6.99
ILMN_1876148 7.09
ILMN_1915152 6.92
ILMN_1886710 7.28
ILMN_1848344 7.03
ILMN_1785340 9.27
ILMN_1779536 7.91
ILMN_1872584 7.01
ILMN_1915587 6.97
ILMN_1654552 11.48
ILMN_1754400 9.33

Total number of rows: 43148

Table truncated, full table size 757 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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