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Items: 3

1.

High Frequency of CNV Mutations in Combined Schizophrenia and Epilepsy

(Submitter supplied) 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.
Organism:
Homo sapiens
Type:
Genome variation profiling by genome tiling array
Platforms:
GPL10807 GPL10806
506 Samples
Download data: TXT
Series
Accession:
GSE23703
ID:
200023703
2.

Agilent-023456 Custom BCM-Beaudet Human 180K V8cleaned aCGH Array

(Submitter supplied) array Comparative Genomic Hybridization (arrayCGH) 180K array with 30kb backbone coverage and exon by exon coverage for 1714 genes reported to be associated with or cause disease v8 chip after cleaning Arrays of this design have barcodes that begin with 16023456 or 2523456. Orientation: Features are numbered numbered Left-to-Right, Top-to-Bottom as scanned by an Agilent scanner (barcode on the left, DNA on the back surface, scanned through the glass), matching the FeatureNum output from Agilent's Feature Extraction software. more...
Organism:
Homo sapiens
1 Series
483 Samples
Download data
Platform
Accession:
GPL10806
ID:
100010806
3.

Bipolar and Epilepsy-41

Organism:
Homo sapiens
Source name:
lymphobast cell lines (channel 1) blood (channel 2)
Platform:
GPL10806
Series:
GSE23703
Download data: TXT
Sample
Accession:
GSM585072
ID:
300585072
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db=gds|term=GSM585072[Accession]|query=14|qty=2|blobid=MCID_671f9e0ee158b40557c4e2b1|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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