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Sample GSM1006737 Query DataSets for GSM1006737
Status Public on Sep 30, 2015
Title distant normal_stage 2_#3
Sample type RNA
 
Source name colorectal distant normal mucosa, stage 2
Organism Homo sapiens
Characteristics tissue: colorectal distant normal mucosa
histology: Normal mucosa
age: 58
Sex: female
paired_tumor_stage: 2
Extracted molecule total RNA
Extraction protocol On average, 100-150mg of flash frozen sample tissue were prepared for the extraction of total RNA. TRIZOL Reagent (Invitrogen ) were used to extract total RNA according to manufacturer's protocol
Label Cy5
Label protocol 5-μg total RNA was used for Cy5-labeled aRNA preparation using a MessageAmp™ aRNA amplification kit (Ambion, Austin, TX).
 
Hybridization protocol Chips with labeled samples were hybridized at 50°C for overnight in a heat-shrunk hybridization bag (Phalanx), and then washed successively with 2×SSPE/0.2% SDS at 42°C for 5 min, 2×SSC at 42°C for 5 min, 2×SSC at room temperature for 5 min and 0.2×SSC at room temperature for 15 min.
Scan protocol Slides were scanned using a Genepix 4000B laser scanner (Axon, New York) and fluorescent intensities were extracted from the generated images by Genepix Pro 6.0 software (Axon).
Description matched distant normal mucosa come from the same patient marked with identical sample name(I,II,III and IV stands for TNM stage 1,2,3 and 4,respectively, ca stands for tumor, n stands for normal mucosa);sample name with identical stage and number represent the same patient(for example, I-n-2 and I-ca-2 represent the normal mucosa and tumor from patient #2 of stage I,respectively).
Data processing The repeatability of the microarray within each class ( normal, stageI,II,II and IV) were examined by correlation analysis. Only those data with over 50% of intra-class correlation coefficient greater than 0.8 were selected for further analysis(Chen et al., 2007). Data filter: > 50% of the arrays and gene signal > 0 were selected. Normalization was done using per chip median normalization and median array method(Liu et al.,2004) .RVM F-test was applied to screen the dynamic differentially expressed miRNA for the normal and different TNM group(Wright et al., 2003).
 
Submission date Sep 19, 2012
Last update date Sep 30, 2015
Contact name xiayu li
E-mail(s) lixiayu@163.com
Organization name Xiangya third hospital
Department department of gastroenterology
Lab Provincial key lab of non-resolving inflammation and cancer
Street address Yuelu district, Tongzipo road #138
City Changsha
State/province Hunan
ZIP/Postal code 410013
Country China
 
Platform ID GPL6254
Series (2)
GSE41011 Dynamic Transcriptome Analysis Reveal New Prognosis Biomarker in Colorectal Cancer (gene expression)
GSE41015 Dynamic Transcriptome Analysis Reveal New Prognosis Biomarker in Colorectal Cancer

Data table header descriptions
ID_REF
VALUE Normalized signal intensity

Data table
ID_REF VALUE
PH_hs_0000003 4.507793903
PH_hs_0000004 8.909892082
PH_hs_0000006 7.464204788
PH_hs_0000007 10.17211437
PH_hs_0000008 3.437404633
PH_hs_0000009 8.01634407
PH_hs_0000010 11.59525681
PH_hs_0000011 5.787901878
PH_hs_0000012 8.880348206
PH_hs_0000013 6.524867535
PH_hs_0000014 7.583082199
PH_hs_0000018 8.499180794
PH_hs_0000020 13.80361748
PH_hs_0000024 11.10416126
PH_hs_0000027 4.437404633
PH_hs_0000028 11.08773804
PH_hs_0000029 4.922831535
PH_hs_0000031 8.290402412
PH_hs_0000032 5.922831535
PH_hs_0000036 6.715389252

Total number of rows: 13838

Table truncated, full table size 350 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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