NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM472508 Query DataSets for GSM472508
Status Public on Nov 19, 2009
Title 168FARN_rep1
Sample type RNA
 
Source name 168FARN breast primary tumor
Organism Mus musculus
Characteristics tissue type: primary breast tumor
tumor stage: 168FARN
Treatment protocol not applicable
Growth protocol 67NR, 168FARN, 4T07, and 4T1 cells were cultured in medium supplemented with 10% FBS (Fetal Bovine Serum) in a CO2 humidified chamber at 37 °C. Three-month-old female BALB/c mice from Janvier Laboratory were used for cell line injection. 67NR, 168FARN, 4T07, and 4T1 cells (5 × 105) were harvested, rinsed in FBS-free medium, and injected into the fourth mammary fat pad in 100 µl of PBS. 8 mice were injected with 67NR cells, 11 mice were injected with 168FARN cells, 15 mice were injected with 4T07 cells, and 13 were injected mice with 4T1 cells. Primary tumors were excised once the average primary tumor size in each group reached 1- to 2-cm in size (measured at the largest dimension).
Extracted molecule total RNA
Extraction protocol Total RNA was isolated using Trizol total RNA isolation reagent (Invitrogen) according to the manufacturer's protocol.
Label biotin
Label protocol Samples were enzymatically fragmented and biotinylated using the WT Terminal Labeling Kit (Affymetrix)
 
Hybridization protocol Samples were hybridized using Affymetrix hybridization kit materials • Heat cocktails at 99° for 5 minutes, then 42° for 5 minutes centrifuge at max speed for 1 minute (N.B. this deviates from Affy SOP). • Transfer 200μl of hyb solution to each array, then tape holes and parafilm. • Hybridize 16 hours at 45° at 60rpm• Fluidics washing is FS450_0001
Scan protocol Affymetrix Gene ChIP Scanner 3000 7G
Description 168FARN_rep1
Data processing Data were processed using EASANA from GenoSplice technology. GC background correction were applied to probe intensities (core), exon level expression were summarized from the corrected intensities and then quantile normalized.
Probe group file used in analysys: MoEx-1_0-st-v1.r2.pgf
 
Submission date Nov 18, 2009
Last update date Nov 18, 2009
Contact name didier auboeuf
E-mail(s) [email protected]
Phone 33426556745
Organization name inserm
Department u590
Lab centre Léon Bérard
Street address 28 rue Laenec
City lyon
ZIP/Postal code 69008
Country France
 
Platform ID GPL6193
Series (1)
GSE19086 Exon-based clustering of tumor transcriptomes reveals alternative exons associated with metastasis in breast cancer

Data table header descriptions
ID_REF
VALUE Quantile normalized exon level expression values (log2) from EASANA (GenoSplice technology)

Data table
ID_REF VALUE
4304927 2.714906
4304928 11.26261
4304938 7.54423
4304943 6.133605
4304949 8.971938
4304956 6.626813
4304969 13.54492
4304972 6.373882
4304978 10.9741
4304981 7.060189
4304986 5.328018
4304997 6.964515
4305011 2.776093
4305016 5.333504
4305019 4.142012
4305028 8.384706
4305034 12.44852
4305036 10.57607
4305039 6.821966
4305048 9.022078

Total number of rows: 228090

Table truncated, full table size 3761 Kbytes.




Supplementary file Size Download File type/resource
GSM472508.CEL.gz 23.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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