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Series GSE38149 Query DataSets for GSE38149
Status Public on May 01, 2015
Title Copy Number Variants at Chromosome 10q11.21, 12p12.1 and 21q22.11 May Be Associated with Hyperlipidemia in Taiwanese Patients
Organism Homo sapiens
Experiment type SNP genotyping by SNP array
Genome variation profiling by SNP array
Summary Affymetrix SNP array analysis was performed on DNA extracted from whole blood samples of 7 Taiwanese patients with hyperlipidemia. Three copy number variant (CNV) regions associated significantly with hyperlipidemia were identified through genomic segmentation analysis (P<0.001).
 
Overall design 7 male Taiwanese hyperlipidemia patients.
 
Contributor(s) Shia WC
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Submission date May 22, 2012
Last update date Nov 27, 2018
Contact name Wei-Chung Shia
Organization name Changhua Christian Hospital
Department Cancer Research Center
Street address 8F., No.235, Xuguang Rd.
City Changhua City
ZIP/Postal code 500
Country Taiwan
 
Platforms (1)
GPL6801 [GenomeWideSNP_6] Affymetrix Genome-Wide Human SNP 6.0 Array
Samples (7)
GSM935929 Taiwanese hyperlipidemia patient 39
GSM935930 Taiwanese hyperlipidemia patient 41
GSM935931 Taiwanese hyperlipidemia patient 45
Relations
BioProject PRJNA167282

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
GSE38149_RAW.tar 555.3 Mb (http)(custom) TAR (of CEL, CHP, CNCHP)
Processed data included within Sample table
Processed data provided as supplementary file

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