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Sample GSM1063468 Query DataSets for GSM1063468
Status Public on Oct 16, 2014
Title M13M
Sample type genomic
 
Channel 1
Source name metastasis of ccRCC
Organism Homo sapiens
Characteristics tissue: metastasis of ccRCC
age: 71
Sex: female
site: lung
Stage: T1bNxM0
Extracted molecule genomic DNA
Extraction protocol standard proteinase K-digestion method
Label Cy5
Label protocol Agilent Genomic DNA Labeling Kit Plus(Agilent)
 
Channel 2
Source name normal renal cortex
Organism Homo sapiens
Characteristics tissue: normal renal cortex
Sex: female
Extracted molecule genomic DNA
Extraction protocol standard proteinase K-digestion method
Label Cy3
Label protocol Agilent Genomic DNA Labeling Kit Plus(Agilent)
 
 
Hybridization protocol dissolved in hybridization buffer (Agilent Oligo aCGH Hybridization Kit; Agilent Technologies), denatured and hybridized to the CGH array at 65C for 24 h
Scan protocol A microarray was scanned using Microarray acanner (Agilrny Technologies) at a pixel resolution size of 5μm
Description normal renal cortex obtained from each patient was used as the source of control DNA
Data processing Microarray images were analyzed by using FEATURE EXTRACTION v.9.1.3.1, v.9.5.1.1 or v.9.5.3.1 (Agilent Technologies) with linear normalization (protocol CGH-v4_91 or CGH-v4_95_Feb07), and the resulting data were subsequently imported into the DNA Analytics v.4.0.81 software package (Agilent Technologies). Following normalization of the raw data, the log2ratio of Cy5 (tumor) to Cy3 (Control) was calculated. Aberrant regions were determined by the Aberration Detection Method-2 algorithm at a threshold of 6.0 in DNA Analytics. To detect gains and losses of chromosomal regions, we set the values of parameters for aberration filters as follows: minimum number of probes in region 2, minimum absolute average log2ratio for region 0.10, maximum number of aberrant regions 10000, and percentage penetrance per feature 0.
 
Submission date Jan 14, 2013
Last update date Oct 17, 2014
Contact name Takahiro Narimatsu
Organization name Oita University
Department Medicine
Lab Molecular Pathology
Street address Hasamamachi Idaigaoka 1-1
City Yufu
State/province Oita
ZIP/Postal code 8795503
Country Japan
 
Platform ID GPL8841
Series (1)
GSE43477 Genomic profiling of primary and metastatic clear cell renal cell carcinoma by array-based comparative genomic hybridization.

Data table header descriptions
ID_REF
VALUE log2 normalized ratio tumor/normal

Data table
ID_REF VALUE
A_14_P112718 0.20753872
A_14_P201353 -0.32451004
A_14_P108353 -0.54442066
A_14_P129881 -0.36840305
A_14_P114030 -0.094688214
A_14_P139527 0.27929044
A_14_P118340 0.14247236
A_14_P106890 0.0387243
A_14_P122641 0.007058101
A_14_P107170 -0.2814795
A_14_P100766 0.33857772
A_14_P118104 -0.32387233
A_14_P117253 -0.32373774
A_14_P129407 -0.3224699
A_14_P200001 -0.2057378
A_14_P103811 -0.040574063
A_14_P119666 0.5490566
A_14_P100799 -0.11962091
A_14_P121179 0.37048542
A_14_P115318 -0.1541588

Total number of rows: 42416

Table truncated, full table size 1009 Kbytes.




Supplementary file Size Download File type/resource
GSM1063468_M13M_FEATURE_EXTRACTION_v.9.5.3.1_Protocol_CGH-v4_95_Feb07.txt.gz 13.1 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data are available on Series record

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