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Series GSE72668 Query DataSets for GSE72668
Status Public on Nov 30, 2015
Title Rare CNVs in Lynch Syndrome patients negative for mutations in mismatch repair genes
Organism Homo sapiens
Experiment type Genome variation profiling by genome tiling array
Genome variation profiling by SNP array
Summary This SuperSeries is composed of the SubSeries listed below.
 
Overall design Refer to individual Series
 
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Submission date Sep 02, 2015
Last update date Jul 13, 2018
Contact name Rolando Andre Rios Villacis
E-mail(s) rolando.andre@unb.br
Phone +5561996912223
Organization name University of Brasília - UnB
Department Genetics and Morphology
Lab Genetic Toxicology
Street address Asa Norte
City Brasília
State/province DF
ZIP/Postal code 70910-900
Country Brazil
 
Platforms (2)
GPL10150 Agilent-022060 SurePrint G3 Human CGH Microarray 4x180K (Probe Name version)
GPL16131 [CytoScanHD_Array] Affymetrix CytoScan HD Array
Samples (67)
GSM1867861 Patient 1 [Agilent]
GSM1867863 Patient 2 [Agilent]
GSM1867865 Patient 3 [Agilent]
This SuperSeries is composed of the following SubSeries:
GSE72665 Rare CNVs in Lynch Syndrome patients negative for mutations in mismatch repair genes [Agilent]
GSE72667 Rare CNVs in Lynch Syndrome patients negative for mutations in mismatch repair genes [Affymetrix]
Relations
BioProject PRJNA294618

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
GSE72668_RAW.tar 4.8 Gb (http)(custom) TAR (of CEL, CYCHP, TXT)

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