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Sample GSM1162259 Query DataSets for GSM1162259
Status Public on Dec 31, 2014
Title colonic mucosal biopsy from left-sided colitis 12
Sample type RNA
 
Source name Colonic mucosal biopsy from patient with left-sided coltis
Organism Homo sapiens
Characteristics tissue: Colonic mucosal biopsy from the left side of the colon
disease state: left-sided coltis
Extracted molecule total RNA
Extraction protocol RNA was extracted with the NucleoSpin® RNA/Protein mini kit (Macherey-Nagel, Düren, Germany) in accordance with the manufactures protocol. Integrity (only samples with a RNA integrity number above 7 were included) and purity were verified with an Agilent Bioanalyzer (Palo Alto, CA, USA).
Label Biotin
Label protocol In accordance with the Affymetrix protocol and the one-cycle eukaryotic target labelling assay, biotin-labelled cRNA was produced
 
Hybridization protocol The cRNA was fragmented and a hybridization mix was prepared, which included the fragmented target, probe array controls, bovine serum albumin, and herring sperm DNA. In this experiment, the Affymetrix GeneChip Human Genome U133 Plus 2.0 was applied.
Scan protocol The hybridized probe array was subsequently stained with fluorescent protein streptavidin-phycoerythirn and scanned with a GeneArray scanner at the excitation wavelength of 488 nm. The amount of light emitted at 570 nm was proportional to the bound target at each location on the probe array.
Data processing By employing the robust multi-array analysis procedure with quantile normalization implemented in the Affymetrix library for the R statistical environment, a single log2 scale expression measure for each probe set was attained from the low level data files (CEL files). Principal component analysis (PCA) was used in order to reduce data complexity. This was performed with the R package pcaGoPromoter, The Hotelling T2 test, which is the multivariate counterpart of a Student’s t-test, was conducted on the two-component PCA model. In brief the scores for each sample were applied to a multiple linear regression model using a dummy variable to encode the classes (left-sided colitis, pancolitis, and dysplasia, respectively). The calculations were performed in R. Dysplasia was tested against pancolitis and left-sided colitis, respectively.
 
Submission date Jun 13, 2013
Last update date Dec 31, 2014
Contact name Jacob Tveiten Bjerrum
E-mail(s) bjerrum.jacob@gmail.com
Phone +45 38681059
Organization name Herlev Hospital
Department Department of Gastroenterology, Medical Section
Street address Herlev Ringvej 75
City Herlev
ZIP/Postal code 2730
Country Denmark
 
Platform ID GPL570
Series (1)
GSE47908 Transcriptional analysis of left-sided colitis, pancolitis and ulcerative colitis-associated dysplasia

Data table header descriptions
ID_REF
VALUE log2 RMA signal

Data table
ID_REF VALUE
1007_s_at 10.8743686190464
1053_at 7.55567163784076
117_at 6.41060645631223
121_at 8.47135570827428
1255_g_at 3.41891382975245
1294_at 8.74570319875378
1316_at 4.69010551062237
1320_at 5.23944224988133
1405_i_at 8.19153906511995
1431_at 3.95730710779419
1438_at 7.58285125287699
1487_at 8.96779439897047
1494_f_at 5.61704476893702
1552256_a_at 8.38168285465127
1552257_a_at 9.85756331302358
1552258_at 4.86103363908787
1552261_at 5.0119910068825
1552263_at 7.60493230375777
1552264_a_at 8.92849928292716
1552266_at 3.92642295035094

Total number of rows: 54675

Table truncated, full table size 1479 Kbytes.




Supplementary file Size Download File type/resource
GSM1162259_Left_12.CEL.gz 8.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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