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Sample GSM1096625 Query DataSets for GSM1096625
Status Public on Aug 25, 2017
Title Fatty changes of liver CR563039
Sample type RNA
Source name Fatty changes of Liver
Organism Homo sapiens
Characteristics project id: 4610
facility id: 46239  
sample id: CR563039
tissue: liver
gender: male
age: 56
paired: F
260/280: 2.2
260/230: 2.1
rin: 9.4
disease state: Fatty changes of liver
Treatment protocol No treatment was involved with any of the patients.
Extracted molecule total RNA
Extraction protocol Homogenized lysate of human tissues (i.e. hepatocellular carcinoma, cirrhotic, and liver) were processed to obtain about 5 mg of high-quality total RNA using a RNeasy Midi Kit (QIAGEN, Valencia, CA, USA). The samples were obtained via tissue biorepository (OriGene Technologies, Inc., Rockville, MD, USA). The RNA integrity and quality control of 2 mL sample was assessed with NanoDrop® ND-1000 UV spectrophotometer and Agilent® 2100 Bioanalyzer at the Molecular Profiling Facility at the University of Pennsylvania. Degraded samples were eliminated from the study based on the OD A260/A280 ratios, electrophoresis results, 28S/18S rRNA ratios, and RNA Integrity Number (RIN).
Label biotin allonamide triphosphate
Label protocol Biotin Allonamide Triphosphate was used according to the standard Affymetrix protocol provided in 2012. The Ambion® WT Expression kit was used as suggested by the manufacturer to generate sense strand cDNA from 250 ng total RNA followed by fragmentation and labeling of 5.5 ug of sense strand cDNA with the GeneChip® Wt Terminal labeling kit.
Hybridization protocol Target hybridization was performed on Affymetrix Human GeneChip® Gene 1.0 ST Arrays (Affymetrix, Inc., Santa Clara, CA, USA) according to the manufacturer’s procedures in the GeneChip® Hybridization Oven 645, followed by washing and staining in the GeneChip® Fluidics Station 450.
Scan protocol Data acquired with GeneChip® Scanner 3000 7G (Affymetrix, Inc., Santa Clara, CA, USA)
Description Based on pathologist report of grouping stage IIIA.
Data processing The mean absolute deviation of residuals, mean absolute relative log expression, and the positive versus negative Receiver Operator Curve (ROC) Area under Curve (ROC) of the array data were metrics used to assess the overall data quality. The probe-level data (cel files) from all arrays were imported into Partek Genomics Suite software (Partek Incorporated, St. Louis, MO, USA) where RMA normalization was applied yielding log2-transformed expression intensities.
One-way ANOVA was performed on the genes across the 3 groups to provide p-values, and false positive rates were computed using the Benjamini-Hochberg step-up algorithm as implemented in Partek. Pairwise comparisons were made between tissues types providing p-values, log2 ratios, and fold-change values. Within-patient (i.e. tissues from the same human subject) log2 ratios and fold-changes were also calculated for the 3 patient sample pairs.
Submission date Mar 12, 2013
Last update date Aug 25, 2017
Contact name Moses Morakortoi Darpolor
Phone 2158981805
Organization name University of Pennsylvania
Department Radiology
Street address 423 Guardian Drive
City Philadelphia
State/province PA
ZIP/Postal code 19104
Country USA
Platform ID GPL6244
Series (1)
GSE45050 Expression data from human hepatocellular carcinoma (HCC), Cirrhosis, and non-tumor liver tissues.

Data table header descriptions
VALUE log2 RMA signal

Data table
8033433 11.3896
8052747 7.46912
7964183 9.99538
7905220 8.60714
7928330 10.6578
8097628 9.02282
7958056 9.99538
8147580 8.62347
8159086 8.42358
8114249 10.6962
8132250 8.4165
7961102 9.21366
8106418 12.1504
8079060 8.81856
8113369 9.88877
8090366 10.1676
8054439 8.17345
7922130 7.60347
7920317 10.5678
7920725 8.31873

Total number of rows: 28536

Table truncated, full table size 442 Kbytes.

Supplementary file Size Download File type/resource
GSM1096625_4610_46239_CR563039_HuGene_HuGene-1_0-st-v1_.CEL.gz 4.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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