NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM837764 Query DataSets for GSM837764
Status Public on Nov 27, 2012
Title SpinalCord_GSM463934
Sample type RNA
 
Source name pooled Human spinal cord total RNA
Organism Homo sapiens
Characteristics tissue: spinal cord
ethnicity: caucasian
Extracted molecule total RNA
Extraction protocol Samples of total RNA from Human tissues were purchased from several companies (Clontech, Ambion, Stratagene, Cell Applications). HeLa and SH-SY5Y cells were cultured in standard DMEM / 10% FBS medium. Total RNA was extracted from cells with TRIzol regent (Invitrogen). Additionally, total RNA was purified with Rneasy Mini Kit (Qiagen) and treated with RNase-free DNase Set (Qiagen) to remove any contaminating genomic DNA.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 2 ug total RNA (Expression Analysis Technical Manual, Rev. 3, 2009, Affymetrix).
 
Hybridization protocol Following fragmentation, 10 ug of cRNA were hybridized for 16 hr at 45C on GeneChip Human Genome Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol GeneChips were scanned using the Affymetrix Scanner 3000 7G.
Data processing The data were digitalized using GeneChip Operating Software (GCOS) v.1.3 (Affymetrix).
Gene expression array data were normalized using MAS5 algorithm (Affymetrix). Then, to correct for bias between chips, quantile normalization (Bolstad, B. M. et al. Bioinformatics 19, 185-193 (2003)) was applied to all array data using R software.
The intensities were converted to a logarithmic scale (base 2). Signal reliability of each probe was determined based on the MAS5 Call algorithm (Affymetrix), and each probe was assigned to one of three flags (P: present, M: marginal, and A: absent).
 
Submission date Nov 21, 2011
Last update date Nov 27, 2012
Contact name Fuyuki Miya
E-mail(s) [email protected]
Phone +81-3-5363-3890
Organization name Keio University
Department School of Medicine
Lab Center for Medical Genetics
Street address 35 Shinanomachi, Shinjuku-ku
City Tokyo
State/province Tokyo
ZIP/Postal code 160-8582
Country Japan
 
Platform ID GPL570
Series (1)
GSE33846 Expression data of hepatocytes isolated from chimeric mouse livers repopulated with human hepatocytes and from normal human livers
Relations
Reanalysis of GSM463934

Data table header descriptions
ID_REF
VALUE log2 quantile normalized data
ABS_CALL

Data table
ID_REF VALUE ABS_CALL
1007_s_at 13.29 P
1053_at 8.14 P
117_at 7.94 P
121_at 8.84 P
1255_g_at 6.44 P
1294_at 8.81 P
1316_at 6.56 P
1320_at 6.11 A
1405_i_at 7.83 P
1431_at 6.76 P
1438_at 6.55 A
1487_at 8.67 P
1494_f_at 6.77 P
1552256_a_at 9.71 P
1552257_a_at 8.63 P
1552258_at 6.18 A
1552261_at 5.66 A
1552263_at 6.98 P
1552264_a_at 9.74 P
1552266_at 5.92 A

Total number of rows: 54675

Table truncated, full table size 958 Kbytes.




Supplementary file Size Download File type/resource
GSM837764.CEL.gz 8.0 Mb (ftp)(http) CEL
Processed data included within Sample table

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