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Series GSE23703 Query DataSets for GSE23703
Status Public on Dec 31, 2010
Title High Frequency of CNV Mutations in Combined Schizophrenia and Epilepsy
Organism Homo sapiens
Experiment type Genome variation profiling by genome tiling array
Summary Agilent custom designed array comparative genomic hybridization (CGH) was performed on 235 samples with a dual diagnosis of schizophrenia and epilepsy and 80 samples with a dual diagnosis of bipolar and epilpsy. ArrayCGH on 191 psychiatric screened controls was also performed. A common male reference was used for all samples and controls. Samples and controls were obtained from the NIMH cell line repositories.
 
Overall design 235 samples with a dual diagnosis of schizophrenia and epilepsy, 80 samples with a dual diagnosis of bipolar and epilepsy, and 191 psychiatric screened controls
 
Contributor(s) Beaudet A, Burant-Hall A, Stewart L
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Submission date Aug 18, 2010
Last update date Mar 22, 2012
Contact name April Burant Hall
Organization name Baylor College of Medicine
Department Molecular and Human Genetics
Lab Dr. Arthur Beaudet
Street address One Baylor Plaza
City Houston
State/province TX
ZIP/Postal code 77030
Country USA
 
Platforms (2)
GPL10806 Agilent-023456 Custom BCM-Beaudet Human 180K V8cleaned aCGH Array
GPL10807 Agilent-026570 Custom BCM-Beaudet Human 180K V8.1 Superfinal aCGH Array
Samples (506)
GSM584606 Control-1
GSM584607 Control-2
GSM584608 Control-3
Relations
BioProject PRJNA130899

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE23703_RAW.tar 9.3 Gb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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