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Series GSE95488 Query DataSets for GSE95488
Status Public on Mar 01, 2017
Title Wilms Tumor in Beckwith-Wiedemann Syndrome and Loss of Methylation at Imprinting Centre 2
Organism Homo sapiens
Experiment type Genome variation profiling by SNP array
SNP genotyping by SNP array
Methylation profiling by genome tiling array
Summary This SuperSeries is composed of the SubSeries listed below.
 
Overall design Refer to individual Series
 
Citation(s) 28699632
Submission date Feb 28, 2017
Last update date Mar 22, 2019
Contact name Jack Brzezinski
E-mail(s) jack.brzezinski@mail.utoronto.ca
Organization name University of Toronto
Street address 555 University Avenue
City Toronto
State/province ON
ZIP/Postal code M5G1X8
Country Canada
 
Platforms (2)
GPL13534 Illumina HumanMethylation450 BeadChip (HumanMethylation450_15017482)
GPL20641 Illumina HumanOmni2.5M-8v1-1_B [data table]
Samples (26)
GSM2515099 Blood Sample Case 1 [SNP]
GSM2515100 Blood Sample Case 2 [SNP]
GSM2515101 Control Blood Sample EP52
This SuperSeries is composed of the following SubSeries:
GSE95484 Wilms Tumor in Beckwith-Wiedemann Syndrome and Loss of Methylation at Imprinting Centre 2 [HumanOmni2.5M]
GSE95486 Wilms Tumor in Beckwith-Wiedemann Syndrome and Loss of Methylation at Imprinting Centre 2 [450K Methylation Array]
Relations
BioProject PRJNA377262

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
GSE95488_RAW.tar 783.7 Mb (http)(custom) TAR (of IDAT)

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