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Series GSE62440 Query DataSets for GSE62440
Status Public on Oct 17, 2014
Title Application of CGH-array and SNP-array for the detection of genomic rearrangements responsible for sindromic mental retardation of unknown cause
Organism Homo sapiens
Experiment type Genome variation profiling by SNP array
Genome variation profiling by array
Summary This SuperSeries is composed of the SubSeries listed below.
 
Overall design Refer to individual Series
 
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Submission date Oct 16, 2014
Last update date Nov 27, 2018
Contact name Francisco Martinez
E-mail(s) martinez_fracas@gva.es
Organization name Hospital Universitari i Politecnic La Fe
Department Unidad de Genetica
Street address Avenida Campanar 21
City Valencia
State/province Valencia
ZIP/Postal code 46009
Country Spain
 
Platforms (3)
GPL6801 [GenomeWideSNP_6] Affymetrix Genome-Wide Human SNP 6.0 Array
GPL8841 Agilent-014950 Human Genome CGH Microarray 4x44K (Probe Name version)
GPL19303 Agilent-035925 microSOPHIA3.0 (4X44K)
Samples (5)
GSM1527005 Human Male with Syndromic Intellectual disability_SNP-array
GSM1527006 Human Male with Syndromic Intellectual disability_1_CGH-array
GSM1527007 Human Female with Syndromic Intellectual disability_1_CGH-array
This SuperSeries is composed of the following SubSeries:
GSE62438 Application of SNP-array for the detection of genomic rearrangements responsible for sindromic mental retardation of unknown cause
GSE62439 Application of CGH-array for the detection of genomic rearrangements responsible for sindromic mental retardation of unknown cause
Relations
BioProject PRJNA264094

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
GSE62440_RAW.tar 114.0 Mb (http)(custom) TAR (of CEL, CNCHP, TXT)

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