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Sample GSM663738 Query DataSets for GSM663738
Status Public on Jan 31, 2011
Title N019, normal pituitary, biological rep 3
Sample type RNA
 
Source name Normal human pituitary obtained at autopsy within 2 - 18 hours of death
Organism Homo sapiens
Characteristics tissue (group): Normal pituitary
gender: F
subclass: N/A
invasive: N/A
recurrent: N/A
scan_date: 2004-07-01
Treatment protocol With informed consent, pituitary tumor samples were obtained from patients at University of Colorado Hospital at the time of transsphenoidal surgery. Portions of the specimens not used for histology and immunohistochemistry were placed in RNAlater and stored at -80C. Gonadotrope tumors were defined as demonstrating positive immunostaining for FSH, LH, or alpha subunit in greater than 5-10% of cells. Null cell adenomas were defined by gonadotropic staining for FSH, LH, or alpha subunit in less than 5-10% of cells. Normal pituitary glands used as controls were obtained at autopsy within 2 - 18 hours of death from University of Colorado Denver Pathology Department.
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol Microarray targets were prepared and labeled from 300ng of total RNA using the MessageAmp Premier RNA Amplification Kit (Applied Biosystems/Ambion, Austin, TX) following the manufactures instructions.
 
Hybridization protocol standard Affymetrix procedures
Scan protocol standard Affymetrix procedures, using the Affy GCS3000
Data processing Hybridization intensities were quantified and normalized across all arrays using the RMA algorithm with GC adjust available as an array processing tool on Partek® Genomics Suite™ 6.5 software (St.Louis, MS). Data were filtered to remove all genes considered absent, as determined by the Affymetrix GeneChip Operating Software (GCOS), in greater than 95% of all the samples (22 out of 23 total samples). Remaining transcripts (38,932 of 54,675) were used for all subsequent statistical and visual analysis. A mixed model ANOVA was employed to estimate the batch effect and the data were adjusted using the Partek Batch Remover™ tool available on Partek Genomics Suite.
 
Submission date Jan 31, 2011
Last update date Jan 31, 2017
Contact name Michael Edwards
E-mail(s) [email protected]
Phone 303-724-6054
Organization name UC Denver
Department Pulmonary
Street address 12700 East 19th Avenue, Box C272
City Aurora
State/province CO
ZIP/Postal code 80045
Country USA
 
Platform ID GPL570
Series (1)
GSE26966 Identification of Growth arrest and DNA-damage-inducible gene beta (GADD45beta) as a Novel Tumor Suppressor in Pituitary Gonadotrope Tumors
Relations
Reanalyzed by GSE68015
Reanalyzed by GSE94349

Data table header descriptions
ID_REF
VALUE GCRMA-calculated signal intensity (log2)

Data table
ID_REF VALUE
1007_s_at 9.98737
1053_at 5.3821
117_at 3.11762
121_at 4.80216
1294_at 3.74612
1316_at 4.16829
1405_i_at 4.4192
1431_at 2.44717
1438_at 1.7517
1487_at 4.92621
1494_f_at 2.17392
1552256_a_at 7.61747
1552257_a_at 7.18265
1552261_at 2.16411
1552263_at 4.48311
1552264_a_at 5.04981
1552266_at 2.54342
1552269_at 2.34246
1552272_a_at 2.00565
1552274_at 6.96557

Total number of rows: 38932

Table truncated, full table size 711 Kbytes.




Supplementary file Size Download File type/resource
GSM663738.CEL.gz 4.6 Mb (ftp)(http) CEL
Processed data included within Sample table

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