NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1082776 Query DataSets for GSM1082776
Status Public on Feb 14, 2013
Title Normal colon tissue, NBRCCC015
Sample type genomic
 
Channel 1
Source name Normal colon tissue, recurrence-free group
Organism Homo sapiens
Characteristics tissue: normal colon adjacent to colon cancer
age: 48 yr
relapse status: recurrence-free
Growth protocol Tissues were obtained and immediately snap-frozen in liquid nitrogen and stored.
Extracted molecule genomic DNA
Extraction protocol Genomic DNA (gDNA) was prepared using the phenol/chloroform/isoamyl alcohol method.
Label Cy5
Label protocol Labeling was performed according to Agilent's recommended protocol. Briefly, 5 μg gDNA was digested with restriction enzymes Alu I (Promega) and Rsa I (Promega), and was labeled fluorescently using the Agilent DNA Labeling kit (Agilent). Patients' gDNAs were labeled with Cy5 and commercial gDNAs as a reference were labeled with Cy3 dUTP, respectively.
 
Channel 2
Source name Commerical gDNA
Organism Homo sapiens
Characteristics sample type: reference
Extracted molecule genomic DNA
Extraction protocol Control DNA: Promega #G1471 (male) and #G1521 (female).
Label Cy3
Label protocol Labeling was performed according to Agilent's recommended protocol. Briefly, 5 μg gDNA was digested with restriction enzymes Alu I (Promega) and Rsa I (Promega), and was labeled fluorescently using the Agilent DNA Labeling kit (Agilent). Patients' gDNAs were labeled with Cy5 and commercial gDNAs as a reference were labeled with Cy3 dUTP, respectively.
 
 
Hybridization protocol The labeled DNA was denatured and pre-annealed with Cot-1 DNA and Agilent blocking reagent and hybridized for 40 hours at 20 rpm in an Agilent hybridization oven.
Scan protocol The arrays were scanned at 5-㎛ resolution using an Agilent scanner (Agilent), and the image was analyzed with Feature Extraction Software 9.1.1.1.
Images were quantified using Agilent Feature Extraction Software.
Description NBRCCC015
Data processing Agilent Feature Extraction Software was used for background subtraction and LOWESS normalization.
 
Submission date Feb 13, 2013
Last update date Feb 14, 2013
Contact name Park Chan Hee
E-mail(s) haema@yuhs.ac
Phone 80222277650
Organization name Cancer Metastasis Research Center
Street address Shinchondong 134
City Seodaemun-gu
State/province Seoul
ZIP/Postal code 120-752
Country South Korea
 
Platform ID GPL8841
Series (1)
GSE44300 DNA profiling of human normal colon tissues

Data table header descriptions
ID_REF
VALUE Normalized log10 ratio (Cy5/Cy3) representing test/reference

Data table
ID_REF VALUE
A_14_P100000 0.014632324
A_14_P100001 -0.045679823
A_14_P100002 0.209337935
A_14_P100003 0.227188557
A_14_P100004 -0.276080668
A_14_P100005 -0.005670245
A_14_P100006 0.292696089
A_14_P100007 0.12269152
A_14_P100008 -0.222898215
A_14_P100009 -0.156179696
A_14_P100010 0.236307234
A_14_P100011 0.11349076
A_14_P100012 -0.312745303
A_14_P100013 0.600890577
A_14_P100014 0.183404937
A_14_P100015 -0.587200344
A_14_P100016 -0.049409635
A_14_P100017 -0.090328589
A_14_P100018 -0.268220156
A_14_P100019 -0.168745831

Total number of rows: 42424

Table truncated, full table size 1054 Kbytes.




Supplementary file Size Download File type/resource
GSM1082776_NBRCCC015.txt.gz 14.2 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap