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Series GSE47357 Query DataSets for GSE47357
Status Public on May 24, 2016
Title Normalization of whole-genome SNP data from non-Hodgkin lymphoma patients for copy number variation.
Organism Homo sapiens
Experiment type SNP genotyping by SNP array
Genome variation profiling by SNP array
Summary With the whole genome SNPs array information, we could evaluate the copy number variation of samples so as to find out specific DNA aberrations in non-Hodgkin lymphma comparing with reactive hyperplasia patients.
 
Overall design To find out lymphoma-related copy number variations in 45 non-Hodgkin lymphoma patients comparing with 8 reactive hyperplasia patients.
 
Contributor(s) Zhao W
Citation(s) 24586676
Submission date May 24, 2013
Last update date Mar 27, 2017
Contact name Fan YANG
E-mail(s) [email protected]
Organization name Shanghai Institute of Hematology
Street address 197, Rui Jin Er Road
City Shanghai
ZIP/Postal code 200025
Country China
 
Platforms (2)
GPL8887 Illumina Human610-Quad v1.0 BeadChip
GPL8888 Illumina Human660W-Quad v1.0 BeadChip
Samples (53)
GSM1148081 TCL Patient No.12, lymph node sample
GSM1148082 TCL Patient No.13, lymph node sample
GSM1148083 TCL Patient No.14, lymph node sample
Relations
BioProject PRJNA205289

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
GSE47357_Matrix_signal_610w.txt.gz 232.0 Mb (ftp)(http) TXT
GSE47357_Matrix_signal_660w.txt.gz 58.9 Mb (ftp)(http) TXT
Processed data included within Sample table

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