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Series GSE178887 Query DataSets for GSE178887
Status Public on Dec 29, 2021
Title Epigenome analysis of doxorubicin-induced cardiotoxicity before and after treatemt of breast cancer patients
Organism Homo sapiens
Experiment type Methylation profiling by array
Summary This study aimed to determine whether methylation signature of peripheral blood mononuclear cells (PBMCs) prior to the start of the first cycle of DOX-based chemotherapy could predict the risk of cardiotoxicity in breast cancer patients as well as determine if DOX treatment changed methlation profiles. The Illumina Infinium 450 Human DNA methylation Beadchip was used to obtain DNA methylation profiles across approximately 450k CpGs PBMCs samples before and after treatment. Samples included 10 samples from patients with normal ejection fraction after DOX treatment, 9 samples from patients with abnormal ejection fraction (indicative of cardiotoxicity) after DOX treatment.
 
Overall design Bisulphite converted DNA from the 37 samples were hybridised to the Illumina Infinium 450k Human Methylation Beadchip
 
Contributor(s) Bauer MA, Todorova VK
Citation(s) 34944912
Submission date Jun 25, 2021
Last update date Dec 30, 2021
Contact name Michael Anton Bauer
E-mail(s) mbauer2@uams.edu
Organization name University of Arkansas for Medical Sciences
Department Biomedical Informatics
Street address 4301 W Markham Slot 782
City Little Rock
State/province United States
ZIP/Postal code 72205
Country USA
 
Platforms (1)
GPL13534 Illumina HumanMethylation450 BeadChip (HumanMethylation450_15017482)
Samples (37)
GSM5399938 genomic DNA from PBMC 1
GSM5399939 genomic DNA from PBMC 2
GSM5399940 genomic DNA from PBMC 3
Relations
BioProject PRJNA741405

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
GSE178887_RAW.tar 183.1 Mb (http)(custom) TAR
GSE178887_signal_intensities.txt.gz 85.8 Mb (ftp)(http) TXT
Processed data included within Sample table

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