GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
Series GSE33598 Query DataSets for GSE33598
Status Public on Nov 11, 2011
Title Genomic exploration of monozygotic twins discordant (MZD) for schizophrenia uncovers de novo mutations (DNM) and reveals candidate genes
Organism Homo sapiens
Experiment type Genome variation profiling by SNP array
SNP genotyping by SNP array
Summary We examined six pairs of monozygotic twins discordant (MZD) for schizophrenia and identified copy number variation (CNV) and single nucleotide polymorphism (SNP) differences between affected and unaffected co-twins using the Affymetrix Genome Wide SNP 6.0.
Overall design Affymetrix SNP arrays were performed according to the manufacurer's protocol on DNA extracted from whole blood
CNV analysis was done using Affymetrix Genotyping Console 4.0 and Partek Genotyping Suite
Contributor(s) Castellani CA, Singh SM
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date Nov 09, 2011
Last update date Nov 27, 2018
Contact name Christina A Castellani
Organization name The University of Western Ontario
Department Biology
Street address Biological and Geological Sciences Building
City London
State/province Ontario
ZIP/Postal code N6A5B7
Country Canada
Platforms (1)
GPL6801 [GenomeWideSNP_6] Affymetrix Genome-Wide Human SNP 6.0 Array
Samples (12)
GSM830483 2585 (Twin Pair 1, affected)
GSM830484 2586 (Twin Pair 1, unaffected)
GSM830485 2587 (Twin Pair 2, affected)
BioProject PRJNA148543

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
GSE33598_RAW.tar 519.3 Mb (http)(custom) TAR (of CEL, CHP)
Processed data included within Sample table
Processed data provided as supplementary file

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