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Sample GSM1362606 Query DataSets for GSM1362606
Status Public on Nov 03, 2014
Title 91_52070900803929090410408220338890
Sample type RNA
 
Source name Breast cancer metastasis
Organism Homo sapiens
Characteristics sample type: Fine-needle aspirate
anatomical site: Skin
pam50 subtype: Normal
esr1 module tertile: 1
erbb2 module tertile: 0
aurka module tertile: 0
plau module tertile: 2
vegf module tertile: 0
stat1 module tertile: 2
casp3 module tertile: 0
ras module tertile: 1
mapk module tertile: 2
pten module tertile: 0
akt/mtor module tertile: 0
igf1 module tertile: 0
src module tertile: 2
myc module tertile: 0
e2f3 module tertile: 0
betac module tertile: 1
pik3ca module tertile: 1
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol Samples are processed in parallel in 96-well plates to minimize potential variation. Reaction purification is achieved using magnetic binding beads for cDNA and Qiagen RNeasy kits for cRNA purification. The final in vitro transcription incorporates biotin moieties that are later labeled with phycoerythrin. After amplification, samples are put through a controlled fragmentation to improve hybridization sensitivity and consistency. The labeled molecules are biotinylated-cRNA.
 
Hybridization protocol GeneChip microarrays are loaded with the fragmented target sample/hybridization buffer mix using standard manual techniques. Arrays are hybridized for 18 hours at 45C with vigorous mixing. Unbound sample is removed and staining is accomplished through the binding of streptavidin conjugated phycoerythrin to the hybridized target. Excess label is removed. Washing and staining steps are performed by the Affymetrix FS450 fluidics station using standard protocols.
Scan protocol Arrays are scanned using a GeneChip Scanner 3000 7G with a 48 array autoloader. The scanner maintains the optimal temperature for the arrays prior to and during scanning.
Description Gene expression data from breast cancer metastasis sampled before commencement of treatment for metastatic disease
Data processing Data were processed in the open source software R using the RMA algorithm as deployed from with the aroma.affymetrix package
 
Submission date Apr 03, 2014
Last update date Nov 03, 2014
Contact name Nicholas Tobin
E-mail(s) tobin.nick@gmail.com
Phone +46 761966368
Organization name Karolinska Institutet
Street address Cancer Center Karolinska
City Stockholm
State/province N/A
ZIP/Postal code 17176
Country Sweden
 
Platform ID GPL10379
Series (1)
GSE56493 Expression data from fine-needle aspiration biopsies of breast cancer metastases from different anatomical sites

Data table header descriptions
ID_REF
VALUE log2 RMA

Data table
ID_REF VALUE
100121619_TGI_at 6.325173344
100121620_TGI_at 7.685032333
100121621_TGI_at 5.697306932
100121622_TGI_at 3.450537624
100121623_TGI_at 9.087607602
100121624_TGI_at 9.585241398
100121625_TGI_at 8.289759324
100121626_TGI_at 3.855033362
100121627_TGI_at 4.459980766
100121628_TGI_at 4.580481662
100121629_TGI_at 8.763729103
100121630_TGI_at 4.082741552
100121631_TGI_at 3.896205231
100121632_TGI_at 7.489305521
100121633_TGI_at 8.054337909
100121634_TGI_at 3.63585197
100121635_TGI_at 7.199046966
100121636_TGI_at 4.891543852
100121637_TGI_at 5.450487598
100121638_TGI_at 4.237677631

Total number of rows: 52378

Table truncated, full table size 1482 Kbytes.




Supplementary file Size Download File type/resource
GSM1362606__52070900803929090410408220338890.CEL.gz 5.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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