NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM812364 Query DataSets for GSM812364
Status Public on Mar 16, 2012
Title Autoantibody profiling of normal sample 28
Sample type other
 
Source name Human Blood
Organism Homo sapiens
Characteristics individual: healthy control
tissue: Plasma/Serum
Treatment protocol Precleared Plasma/serum samples were diluted in Washing Buffer and applied to the protein array for the autoantibodyome profiling. The probed protein microarrays were dried and scanned with the Genepix 4200AL Microarray Scanner the Genepix Pro 6.1 software. All probing conditions and procedure was followed as described in invitrogen website. (http://tools.invitrogen.com/content/sfs/manuals/protoarrayIRBP_short_protocol.pdf)
Extracted molecule other
Extraction protocol Precleared Plasma/serum samples were diluted in Washing Buffer and applied to the protein array
Label Alexa Fluor 647
Label protocol All probing conditions and procedure was followed as described in invitrogen website. (http://tools.invitrogen.com/content/sfs/manuals/protoarrayIRBP_short_protocol.pdf)
 
Hybridization protocol All probing conditions and procedure was followed as described in invitrogen website. (http://tools.invitrogen.com/content/sfs/manuals/protoarrayIRBP_short_protocol.pdf)
Scan protocol The probed protein microarrays were dried and scanned with the Genepix 4200AL Microarray Scanner the Genepix Pro 6.1 software.
Description MDS_N28_0000022675.gpr
Data processing The arrays were scanned to obtain signal location, intensity quantification and identification information using GenePix Pro 6.1. For each array inter-array normalization was performed via the ProCAT algorithm (sliding window of length 15). The arrays were then quantile normalized and a comparison of intensities of probes was carried out between the subject and the healthy control group using a two-tailed Mann-Whitney non-parametric test, P<0.01, in Mathematica 8.0 and using Benjamini-Hochberg to correct for multiple hypothesis tests, adjusted P<0.01.
 
Submission date Oct 07, 2011
Last update date Mar 16, 2012
Contact name Hogune Im
Phone 650-723-3277
Organization name Stanford
Department Genetics
Lab Snyder
Street address 300 Pasteur Dr. Alway M308
City Stanford
State/province CA
ZIP/Postal code 94305
Country USA
 
Platform ID GPL14689
Series (2)
GSE32691 Autoantibody profile timecourse of UNK
GSE33029 Integrated analysis of omics profiles

Data table header descriptions
ID_REF
VALUE normalized signal

Data table
ID_REF VALUE
1_i1 11242.34849
2_i2 11576.19992
3_i1 526.8848583
4_i2 538.3473591
5_i1 258.8004106
6_i2 463.4037991
7_i1 1613.735188
8_i2 1554.79957
9_i1 10087.89634
10_i2 10340.35315
11_i1 19146.02211
12_i2 17592.43248
13_i1 368.0349754
14_i2 336.7094924
15_i1 1615.749822
16_i2 1692.61251
17_i1 4232.855291
18_i2 3577.54111
19_i1 80.75841489
20_i2 1530.010796

Total number of rows: 23232

Table truncated, full table size 458 Kbytes.




Supplementary file Size Download File type/resource
GSM812364.gpr.gz 2.6 Mb (ftp)(http) GPR
Processed data included within Sample table

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