NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2233698 Query DataSets for GSM2233698
Status Public on Aug 19, 2016
Title Subject 495, region Occipital Visual Cortex
Sample type RNA
 
Source name Occipital Visual Cortex, 69 yr old male
Organism Homo sapiens
Characteristics subject id: 495
age: 69
Sex: male
race: black
postmortem interval minutes: 255
ph: 6.3
clinical dementia rating: 0.5
braak neurofibrillary tangle score: 1
neuropathological category: Normal
average neuritic plaque density: 0
sum of cerad rating scores in multiple brain regions: 0
sum of neurofibrillary tangles density in multiple brain regions: 1
brain region: Occipital Visual Cortex
tissue: post-mortem brain
Treatment protocol N/A
Growth protocol N/A
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from 50 mg tissue aliquots from brain tissue samples, amplified to cRNA, and biotin-labeled for analysis on the Affymetrix U133AB or U133 Plus 2.0 Human genome GeneChip at Gene Logic Inc. (Gaithersburg, MD, USA) using the TRIzol method and RNeasy columns according to protocols from Affymetrix (Santa Clara, CA, USA). The 28S/18S rRNA ratio of isolated RNA was assessed using a Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) Label – biotin label protocol => followed a protocol described in the Gene Logic GeneChip® Analysis Manual (Gaithersburg, USA).
Label biotin
Label protocol followed a protocol described in the Gene Logic GeneChip® Analysis Manual (Gaithersburg, USA).
 
Hybridization protocol followed a protocol described in the Gene Logic GeneChip® Analysis Manual (Gaithersburg, USA).
Scan protocol followed a protocol described in the Gene Logic GeneChip® Analysis Manual (Gaithersburg, USA).
Data processing The raw microarray data was preprocessed using the robust multiarray Average (RMA) method function implemented in the R/Bioconductor package Affy (v1.44) using the default parameters, including quantile normalizion and log2 transformation. RMA normalization was performed separately for each brain region. For 17 brain regions profiled with both 133A and 133B arrays, 133A and 133B arrays were normalized separately and combined afterwards. Finally, the normalized gene expression data was corrected for covariates including sex, PMI (postmortem interval), pH and race using linear regression.
 
Submission date Jul 14, 2016
Last update date Aug 20, 2016
Contact name Bin Zhang
Organization name Icahn School of Medicine at Mount Sinai
Department Genetics and Genomic Sciences
Street address 1470 Madison Avenue
City New York
State/province NY
ZIP/Postal code 10029
Country USA
 
Platform ID GPL96
Series (1)
GSE84422 Molecular Signatures Underlying Selective Regional Vulnerability to Alzheimer's Disease

Data table header descriptions
ID_REF
VALUE RMA normalized and covariate adjusted expression values.

Data table
ID_REF VALUE
1007_s_at 7.1408313
1053_at 3.0924985
117_at 2.9214614
121_at 3.1577544
1255_g_at 2.0051476
1294_at 2.5895234
1316_at 3.1695558
1320_at 2.587893
1405_i_at 3.3048161
1431_at 2.9183446
1438_at 2.5938023
1487_at 4.1945236
1494_f_at 2.9801896
1598_g_at 3.2667749
160020_at 2.9182324
1729_at 3.2173517
1773_at 2.3334806
177_at 2.6932968
179_at 2.3016227
1861_at 2.2803309

Total number of rows: 22283

Table truncated, full table size 453 Kbytes.




Supplementary file Size Download File type/resource
GSM2233698_32160hg133a11.CEL.gz 3.5 Mb (ftp)(http) CEL
Processed data included within Sample table

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