DocumentCode :
1640122
Title :
Signature genes in human heart failure based on gene expression analysis: Can we identify a unique set?
Author :
Wang, Haiying ; Zheng, Huiru
Author_Institution :
Sch. of Comput. & Math., Univ. of Ulster, Newtownabbey
fYear :
2008
Firstpage :
1
Lastpage :
6
Abstract :
Dilated Cardiomyopathy is one of leading courses of heart failure. Recent advances in microarray technology have promised significant advantages in understanding the molecular mechanisms underlying dilated cardiomyopathy and heart failure. Several microarray studies have successfully yielded a set of signature genes associated with heart failure. However, it has been found that the overlap of these heart failure associated genes derived from different experiments is very small. Based on the analysis of two publicly available microarray datasets associated with heart failure with three types of machine learning and statistical prediction models, this paper explores this phenomenon. We found that there is no unique set of genes associated with heart failure. Many sets of genes can achieve very high prediction accuracy. In order to identify biomarkers in human heart failure, it may not be sufficient to just focus a certain number of top genes. Such main candidates should be chosen from the much longer list of genes.
Keywords :
biology computing; cardiology; genomics; learning (artificial intelligence); medical computing; molecular biophysics; statistical analysis; cardiomyopathy molecular mechanism; dilated cardiomyopathy; gene expression analysis; heart failure molecular mechanism; human heart failure signature genes; machine learning; microarray datasets; microarray technology; statistical prediction models; Biomarkers; Cardiology; Failure analysis; Gene expression; Hafnium; Heart; Humans; Machine learning; Muscles; Predictive models;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
BioInformatics and BioEngineering, 2008. BIBE 2008. 8th IEEE International Conference on
Conference_Location :
Athens
Print_ISBN :
978-1-4244-2844-1
Electronic_ISBN :
978-1-4244-2845-8
Type :
conf
DOI :
10.1109/BIBE.2008.4696682
Filename :
4696682
Link To Document :
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