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Sample GSM2234010 Query DataSets for GSM2234010
Status Public on Aug 19, 2016
Title Subject 755, region Anterior Cingulate
Sample type RNA
 
Source name Anterior Cingulate, 87 yr old male
Organism Homo sapiens
Characteristics subject id: 755
age: 87
Sex: male
race: white
postmortem interval minutes: 165
ph: 6.5
clinical dementia rating: 5
braak neurofibrillary tangle score: 6
neuropathological category: definite AD
average neuritic plaque density: 12.16
sum of cerad rating scores in multiple brain regions: 21
sum of neurofibrillary tangles density in multiple brain regions: 26
brain region: Anterior Cingulate
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 6.9614749
1053_at 3.0292966
117_at 3.1385212
121_at 3.2872875
1255_g_at 2.1895999
1294_at 2.8254631
1316_at 3.5045522
1320_at 2.6214282
1405_i_at 3.1941111
1431_at 2.5535893
1438_at 2.4771418
1487_at 3.9304662
1494_f_at 2.8131532
1598_g_at 3.5686707
160020_at 2.8616716
1729_at 3.48655
1773_at 2.0169309
177_at 2.3500903
179_at 2.3939505
1861_at 2.6719464

Total number of rows: 22283

Table truncated, full table size 453 Kbytes.




Supplementary file Size Download File type/resource
GSM2234010_35188hg133a11.CEL.gz 3.3 Mb (ftp)(http) CEL
Processed data included within Sample table

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