NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1924914 Query DataSets for GSM1924914
Status Public on Nov 04, 2015
Title N2_para-carcinoma liver
Sample type RNA
 
Source name para-carcinoma liver
Organism Homo sapiens
Characteristics tissue: para-carcinoma liver
patient diagnosis: hepatocellular carcinoma
Growth protocol Surgical fresh tissues from HCC patients' liver were stored at -80℃.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from about 30 mg tissues with the RNeasy Mini Kit (Qiagen), according to the manufacturer’s instructions. A 2-round amplification was performed with the ExpressArt TRinucleotide mRNA Amplification Kit (AmpTec) according to the manufacturer’s instructions.
Label biotin
Label protocol Samples were enzymatically fragmented and biotinylated using the GeneChip® 3' IVT Express Kit.
 
Hybridization protocol Samples were hybridized using GeneChip® 3' IVT Express Kit according to the manufacturer's instructions. Heat the hybridization cocktails at 99° for 5 minutes, then incubate the probe array filled with Pre-Hybridization Mix at 45℃ for 10 min with rotation. Transfer the cocktails to a 45℃ heat block for 5 min. Spin the hybridization cocktail at maximum speed in a microcentrifuge for 5 minutes to collect any insoluble material from the hybridization mixture. Remove the array from the hybridization oven. Vent the array with a clean pipette tip and extract the Pre-Hybridization Mix from the array with a micropipettor. Refill the array with the appropriate volume of the clarified hybridization cocktail. Place probe array into the hybridization oven, set to 45 °C. Hybridize for 16 hours.
Scan protocol Affymetrix GeneChip® Scanner 3000 (GCS3000)
Data processing Data were processed using Affymetrix Expression ConsoleTM Software Version 1.0 according to the User Guide. RMA analysis mainly includes 4 steps: background correction on the PM values; quantile normalization across all the chips in the experiment; log2 transformation; median polish summarization.
 
Submission date Nov 03, 2015
Last update date Nov 04, 2015
Contact name Huiyong Yin
E-mail(s) [email protected]
Organization name Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences
Street address 320 Yueyang Road, Xuhui District
City Shanghai
ZIP/Postal code 200031
Country China
 
Platform ID GPL16043
Series (1)
GSE74656 Gene expression profiling of Human Hepatocellular Carcinoma tissues

Data table header descriptions
ID_REF
VALUE Quantile normalized gene level expression values from GeneBASE

Data table
ID_REF VALUE
11715100_at 5.37915
11715101_s_at 6.17318
11715102_x_at 5.67989
11715103_x_at 7.06816
11715104_s_at 6.28184
11715105_at 4.28741
11715106_x_at 5.0994
11715107_s_at 5.78122
11715108_x_at 3.65587
11715109_at 4.75421
11715110_at 7.46956
11715111_s_at 8.46837
11715112_at 3.67944
11715113_x_at 8.18426
11715114_x_at 7.92396
11715115_s_at 3.11904
11715116_s_at 5.29355
11715117_x_at 2.87359
11715118_s_at 3.68334
11715119_s_at 6.91516

Total number of rows: 49395

Table truncated, full table size 1033 Kbytes.




Supplementary file Size Download File type/resource
GSM1924914_N2_PrimeView_.CEL.gz 1.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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