NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM887972 Query DataSets for GSM887972
Status Public on Mar 20, 2012
Title CAL 27
Sample type genomic
 
Source name ATCC
Organism Homo sapiens
Characteristics primary site: upper_aerodigestive_tract
histology: carcinoma
histology subtype1: squamous_cell_carcinoma
Treatment protocol None
Growth protocol Cells lines were cultured following growth recommendations from the cell line source vendors. Cells were incubated at 37 ºC at 5% CO2 until 70% confluency was reached. Pellets were harvested 48 hours post media change, flash frozen, and stored at -80 ºC until nucleic acid extraction.
Extracted molecule genomic DNA
Extraction protocol DNA was extracted from frozen cell pellets, containing an average cell count of 4.5 million cells, using the Qiagen Gentra Puregene method following the manufacturers recommendations. Samples were quantified using picogreen on a ThermoScientific Varioskan Flash instrument.
Label Biotin
Label protocol PCR amplification fragments (200 and 1100 bp) are labeled using terminal deoxynucleotidyl transferase following the Affymetrix GenomeWideSNP_6 protocol
 
Hybridization protocol After denaturation, 200ul of sample are injected into a Genome-Wide Human SNP 6.0 array. Arrays are loaded in the GeneChip® Hybridization Oven 640 @ 50 °C temp, rotating arrays @ 60 rpm. Samples are hybridized for 16 to 18 hours.
Scan protocol Genome-Wide Human SNP Array 6.0 are stained using the GeneChip® Fluidics Station 450 and scanned using the GeneChip® Scanner 3000
Description SNP array data from the CCLE
Data processing The raw CEL files were normalized to copy number estimates using a GenePattern pipeline, as described in Cancer Genome Atlas Research Network et al, Nature, 2008, and hg18 Affymetrix probe annotations. Normalized copy number estimates (log2 ratios) were segmented using the Circular Binary Segmentation (CBS) algorithm, followed by median centering of the segment values to a value of zero in each sample.
 
Submission date Mar 06, 2012
Last update date Dec 21, 2012
Contact name Nicolas Stransky
E-mail(s) stransky@broadinstitute.org
URL http://www.broadinstitute.org/ccle
Organization name Broad Institute
Department Cancer Program
Lab Levi Garraway
Street address 7 Cambridge center
City Cambridge
State/province MA
ZIP/Postal code 02118
Country USA
 
Platform ID GPL15315
Series (2)
GSE36138 SNP array data from the Cancer Cell Line Encyclopedia (CCLE)
GSE36139 SNP and Expression data from the Cancer Cell Line Encyclopedia (CCLE)

Data table header descriptions
ID_REF
VALUE For each gene, log2(CN/2) is reported. In case a gene encompasses more than one segment, the value reported is the one that has the highest absolute value.

Data table
ID_REF VALUE
WASH7P -0.7792
OR4F5 -0.7792
LOC100132062 0.0276
OR4F16 0.0276
OR4F3 0.0276
OR4F29 0.0276
MIR1977 0.0276
LOC100288069 0.0276
NCRNA00115 0.0276
LOC643837 0.0276
FAM41C 0.0276
FLJ39609 0.0276
SAMD11 0.0276
NOC2L 0.0276
KLHL17 0.0276
PLEKHN1 0.0276
C1orf170 0.0276
HES4 0.0276
ISG15 0.0276
AGRN 0.0276

Total number of rows: 22519

Table truncated, full table size 305 Kbytes.




Supplementary file Size Download File type/resource
GSM887972.CEL.gz 34.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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