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BIOLOGICAL NETWORK EPITOMES VIA TOPOLOGICAL COMPRESSION

机译:通过拓扑压缩生物网络脑膜

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High-throughput generation of new types of relational biological datasets is creating a demand for network-based signal processing and pattern recognition to provide new insights. Such networks are often too large to interpret visually and too complicated to be explained solely based on local topological properties. Just as signal processing and statistical techniques have been used in traditional, sequential-based biological datasets, so too are methodologies needed to automatically discern patterns in the huge, emerging networks. One way to do this is by transforming these very large networks into discernable epitomes, or abstracts, of the original networks. This work presents an approach for doing this via topological compression. Through capturing nodes' global topologies and subsequent compression, a new network epitome can be derived. Here, this is done with an E. Coli gene regulation network, resulting in biological findings that could not be derived from the local topology of the original network.
机译:新类型的关系生物数据集的高吞吐量生成是对基于网络的信号处理和模式识别的需求,以提供新的见解。这种网络往往太大而无法在视觉上解释并且过于复杂,不能仅基于局部拓扑特性解释。正如在传统的基于顺序的生物数据集中使用的信号处理和统计技术,所以也是在庞大的新兴网络中自动辨别模式所需的方法。这样做的一种方法是通过将这些非常大的网络转换为原始网络的可辨认的末端或摘要。这项工作提出了一种通过拓扑压缩来执行此操作的方法。通过捕获节点的全局拓扑和随后的压缩,可以派生新的网络拓扑组。这里,这是用大肠杆菌基因调控网络完成的,导致生物学发现,无法从原始网络的当地拓扑中得出。

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