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Network Aggregation to Enhance Results Derived from Multiple Analytics

机译:网络聚合以增强来自多个分析的结果

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摘要

The more complex data are, the higher the number of possibilities to extract partial information from those data. These possibilities arise by adopting different analytic approaches. The heterogeneity among these approaches and in particular the heterogeneity in results they produce are challenging for follow-up studies, including replication, validation and translational studies. Furthermore, they complicate the interpretation of findings with wide-spread relevance. Here, we take the example of statistical epistasis networks derived from genome-wide association studies with single nucleotide polymorphisms as nodes. Even though we are only dealing with a single data type, the epistasis detection problem suffers from many pitfalls, such as the wide variety of analytic tools to detect them, each highlighting different aspects of epistasis and exhibiting different properties in maintaining false positive control. To reconcile different network views to the same problem, we considered 3 network aggregation methods and discussed their performance in the context of epistasis network aggregation. We furthermore applied a latent class method as best performer to real-life data on inflammatory bowel disease (IBD) and highlighted its benefits to increase our understanding about IBD underlying genetic architectures.
机译:数据越复杂,从这些数据中提取部分信息的可能性次数越高。这些可能性是通过采用不同的分析方法来产生的。这些方法中的异质性和它们产生的结果中的异质性是对后续研究的挑战,包括复制,验证和翻译研究。此外,它们与广泛的相关性的对结果的解释复杂化。在这里,我们采用衍生自与单核苷酸多态性的基因组 - 宽关联研究的统计简超网络的例子作为节点。即使我们只是处理单个数据类型,即使是单一数据类型,即使是超自然的缺陷问题也遭受了许多缺陷,例如各种分析工具来检测它们,每个分析工具均突出显示外观的不同方面,并在保持假阳性控制方面表现出不同的性质。要将不同的网络视图协调到同一问题,我们考虑了3个网络聚合方法,并在简历网络聚合的上下文中讨论了它们的性能。我们此外,我们将潜在的方法应用于炎症性肠病(IBD)上的现实生活数据,并强调了其利益,以提高我们对IBD基础遗传架构的理解。

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