首页> 外文会议>BioInformatics BioEngineering -BIBE, 2008 8th IEEE International Conference on >Signature genes in human heart failure based on gene expression analysis: Can we identify a unique set?
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Signature genes in human heart failure based on gene expression analysis: Can we identify a unique set?

机译:基于基因表达分析的人类心力衰竭中的签名基因:我们能否确定独特的基因组?

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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.
机译:扩张型心肌病是心力衰竭的主要病程之一。微阵列技术的最新进展有望在了解扩张型心肌病和心力衰竭的分子机制方面具有显着优势。几项微阵列研究已成功产生了一组与心力衰竭相关的签名基因。但是,已经发现,源自不同实验的这些与心力衰竭相关的基因的重叠非常小。在使用三种类型的机器学习和统计预测模型对与心力衰竭相关的两个公开可用的微阵列数据集进行分析的基础上,本文探讨了这种现象。我们发现没有与心力衰竭相关的独特基因集。许多基因集可以达到很高的预测精度。为了鉴定人类心力衰竭中的生物标志物,仅仅关注一定数量的顶级基因可能还不够。此类主要候选基因应从更长的基因列表中选择。

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