首页> 外文期刊>Bioinformatics >ATHENA: the analysis tool for heritable and environmental network associations
【24h】

ATHENA: the analysis tool for heritable and environmental network associations

机译:雅典娜:可遗传和环境网络关联的分析工具

获取原文
获取原文并翻译 | 示例
       

摘要

Motivation: Advancements in high-throughput technology have allowed researchers to examine the genetic etiology of complex human traits in a robust fashion. Although genome-wide association studies have identified many novel variants associated with hundreds of traits, a large proportion of the estimated trait heritability remains unexplained. One hypothesis is that the commonly used statistical techniques and study designs are not robust to the complex etiology that may underlie these human traits. This etiology could include nonlinear gene x gene or gene x environment interactions. Additionally, other levels of biological regulation may play a large role in trait variability. Results: To address the need for computational tools that can explore enormous datasets to detect complex susceptibility models, we have developed a software package called the Analysis Tool for Heritable and Environmental Network Associations (ATHENA). ATHENA combines various variable filtering methods with machine learning techniques to analyze high-throughput categorical (i.e. single nucleotide polymorphisms) and quantitative (i.e. gene expression levels) predictor variables to generate multivariable models that predict either a categorical (i.e. disease status) or quantitative (i.e. cholesterol levels) outcomes. The goal of this article is to demonstrate the utility of ATHENA using simulated and biological datasets that consist of both single nucleotide polymorphisms and gene expression variables to identify complex prediction models. Importantly, this method is flexible and can be expanded to include other types of high-throughput data (i.e. RNA-seq data and biomarker measurements).
机译:动机:高通量技术的进步使研究人员能够以强大的方式检查复杂人类特征的遗传病因。尽管全基因组关联研究已经确定了与数百个性状相关的许多新颖变异,但估计的性状遗传力的很大一部分仍无法解释。一种假设是,常用的统计技术和研究设计对可能构成这些人类特征的复杂病因并不健全。这种病因可能包括非线性的基因x基因或基因x环境相互作用。另外,其他水平的生物调节可能在性状变异中起重要作用。结果:为了满足对可以探索大量数据集以检测复杂磁化率模型的计算工具的需求,我们开发了名为“遗传和环境网络协会分析工具”(ATHENA)的软件包。 ATHENA将各种变量过滤方法与机器学习技术相结合,以分析高通量分类(即单核苷酸多态性)和定量(即基因表达水平)的预测变量,以生成预测分类(即疾病状态)或定量(即疾病)的多变量模型。胆固醇水平)的结果。本文的目的是通过使用由单核苷酸多态性和基因表达变量组成的模拟和生物数据集来证明复杂的预测模型,从而证明ATHENA的实用性。重要的是,该方法是灵活的,并且可以扩展为包括其他类型的高通量数据(即RNA序列数据和生物标志物测量值)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号