NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1110074 Query DataSets for GSM1110074
Status Public on Mar 29, 2013
Title IBC#12 (RNA)
Sample type RNA
 
Source name IBC, core-biopsy
Organism Homo sapiens
Characteristics sample type: IBC
her2: 3+
er: 0
Treatment protocol For tumor samples, 5–20 frozen sections of biopsy (16 μm thick) were manually microdissected. Under the guidance of a pathologist, normal tissue was removed leaving tumor cells comprising greater than 90% of the specimen. For normal breast samples, 40–60 frozen sections of surgical specimen (16 μm thick) were subjected for microdissection manually.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the RNeasy micro kit (Qiagen; Valencia, CA, USA), and quality was characterized with BioAnalyzer (Agilent Technologies; Waldbronn, Germany).
Label Cy3
Label protocol RNA samples were labeled using the Low Input Quick Amp Labeling kit (Agilent Technologies) according to the manufacturer's instructions.
 
Hybridization protocol Cy3-labelled cRNA was fragmented at 60°C for 30 minutes according to the manufacturer's instructions. On completion of the fragmentation reaction, 100 µl of fragmentation mixture were hybridized to Agilent Whole Human Genome Oligo Microarrays (G4112F) for 17 hours at 65°C in a rotating Agilent hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent).
Scan protocol Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner (G2505B) using one color scan setting for 4x44k array slides (Scan resolution 5um, Dye channel is set to Green and Green PMT is set to XDR Hi 100%, XDR Lo 10%).
Description Two technical replicates were integrated with mean.
Data processing Extract tif images using the Feature Extraction software FE9.5 by GE1-v5_95 protocols. Normalization was performed using global-normalization methods. Two technical replicates were integrated with mean.
 
Submission date Mar 28, 2013
Last update date Mar 29, 2013
Contact name Takahiro Kogawa
E-mail(s) tkogawa1@mdanderson.org
Organization name MD Anderson
Department Breast Medical
Street address 1515 Holcomb Blvd
City Houston
State/province TX
ZIP/Postal code 77030
Country USA
 
Platform ID GPL6480
Series (2)
GSE45581 Expression Analysis of Microdissected Inflammatory Breast Cancer
GSE45584 Expression Analysis and Genomic Analysis of Microdissected Inflammatory Breast Cancer

Data table header descriptions
ID_REF
VALUE Processed signal intensity

Data table
ID_REF VALUE
A_23_P100001 3055.014
A_23_P100011 79.888
A_23_P100022 42.444
A_23_P100056 90.22
A_23_P100074 1164.212
A_23_P100092 447.138
A_23_P100103 671.133
A_23_P100111 314.712
A_23_P100127 1118.627
A_23_P100133 487.88
A_23_P100141 312.545
A_23_P100156 414.334
A_23_P100177 12.553
A_23_P100189 61.057
A_23_P100196 3226.454
A_23_P100203 845.59
A_23_P100220 7074.297
A_23_P100240 48.334
A_23_P10025 384.818
A_23_P100263 26073.466

Total number of rows: 40991

Table truncated, full table size 815 Kbytes.




Supplementary file Size Download File type/resource
GSM1110074_US22502616_251485057901_S01_GE1-v5_95_Feb07_1_2.txt.gz 7.8 Mb (ftp)(http) TXT
GSM1110074_US22502616_251485058211_S01_GE1-v5_95_Feb07_1_4.txt.gz 7.7 Mb (ftp)(http) TXT
Processed data included within Sample table

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