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Sample GSM2233935 Query DataSets for GSM2233935
Status Public on Aug 19, 2016
Title Subject 462, region Posterior Cingulate Cortex
Sample type RNA
 
Source name Posterior Cingulate Cortex, 87 yr old male
Organism Homo sapiens
Characteristics subject id: 462
age: 87
Sex: male
race: white
postmortem interval minutes: 350
ph: 6.5
clinical dementia rating: 1
braak neurofibrillary tangle score: 3
neuropathological category: definite AD
average neuritic plaque density: 18.56
sum of cerad rating scores in multiple brain regions: 33
sum of neurofibrillary tangles density in multiple brain regions: 11
brain region: Posterior Cingulate 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 7.3882955
1053_at 2.9884871
117_at 3.2436232
121_at 2.7778773
1255_g_at 1.9534861
1294_at 2.689873
1316_at 3.2396892
1320_at 2.2973104
1405_i_at 2.8036866
1431_at 2.5563553
1438_at 2.1382479
1487_at 3.9120143
1494_f_at 2.6044052
1598_g_at 3.6351544
160020_at 2.5694528
1729_at 3.2711218
1773_at 2.3162845
177_at 2.5207138
179_at 2.3540262
1861_at 2.2968997

Total number of rows: 22283

Table truncated, full table size 453 Kbytes.




Supplementary file Size Download File type/resource
GSM2233935_35085hg133a21.CEL.gz 3.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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