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Sample GSM2233921 Query DataSets for GSM2233921
Status Public on Aug 19, 2016
Title Subject 230, region Posterior Cingulate Cortex
Sample type RNA
 
Source name Posterior Cingulate Cortex, 96 yr old female
Organism Homo sapiens
Characteristics subject id: 230
age: 96
Sex: female
race: white
postmortem interval minutes: 195
ph: 6.7
clinical dementia rating: 0
braak neurofibrillary tangle score: 2
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: 3
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 6.6020707
1053_at 2.8391704
117_at 2.9431184
121_at 3.0880631
1255_g_at 1.9726701
1294_at 2.8386767
1316_at 3.0917575
1320_at 2.342717
1405_i_at 2.9405066
1431_at 2.4772662
1438_at 2.4790887
1487_at 4.1429492
1494_f_at 2.6697109
1598_g_at 3.1056336
160020_at 2.6809086
1729_at 3.3499374
1773_at 2.4011471
177_at 2.534639
179_at 2.3822249
1861_at 2.4990972

Total number of rows: 22283

Table truncated, full table size 453 Kbytes.




Supplementary file Size Download File type/resource
GSM2233921_35043hg133a11.CEL.gz 3.4 Mb (ftp)(http) CEL
Processed data included within Sample table

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