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Series GSE20290 Query DataSets for GSE20290
Status Public on Feb 12, 2013
Title Towards a comprehensive structural variation map of an individual human genome for personalized medicine
Organism Homo sapiens
Experiment type SNP genotyping by SNP array
Genome variation profiling by SNP array
Genome variation profiling by genome tiling array
Summary This SuperSeries is composed of the SubSeries listed below.
Overall design Refer to individual Series
Citation(s) 20482838
Submission date Feb 11, 2010
Last update date Jan 17, 2019
Contact name Andy Pang
Organization name The Centre for Applied Genomics
Lab Stephen W. Scherer
Street address MaRS Centre - East Tower, 101 College Street, Room 14-701
City Toronto
State/province ON
ZIP/Postal code M5G 1L7
Country Canada
Platforms (87)
GPL6801 [GenomeWideSNP_6] Affymetrix Genome-Wide Human SNP 6.0 Array
GPL6983 Illumina Human1Mv1 DNA Analysis BeadChip (Human1Mv1_C)
GPL9857 Agilent/SNU human 24M CGH array, 1 of 24 (Feature Number version)
Samples (100)
GSM508411 HuRef lymphoblastoid cell line_Affymetrix
GSM1082299 HuRef lymphoblastoid cell line_Illumina
GSM1082326 Lymphoblastoid NA18500 Cy3_Agilent244K
This SuperSeries is composed of the following SubSeries:
GSE20275 Affymetrix SNP and CNV data for the HuRef individual
GSE20284 Illumina SNP and CNV data for the HuRef individual
GSE20287 Agilent custom 244K array CGH data for the HuRef individual
BioProject PRJNA189283

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
GSE20290_RAW.tar 7.0 Gb (http)(custom) TAR (of CEL, CHP, GFF, PAIR, TXT)

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