| Literature DB >> 27889536 |
Hyunghoon Cho1, Bonnie Berger2, Jian Peng3.
Abstract
The topological landscape of molecular or functional interaction networks provides a rich source of information for inferring functional patterns of genes or proteins. However, a pressing yet-unsolved challenge is how to combine multiple heterogeneous networks, each having different connectivity patterns, to achieve more accurate inference. Here, we describe the Mashup framework for scalable and robust network integration. In Mashup, the diffusion in each network is first analyzed to characterize the topological context of each node. Next, the high-dimensional topological patterns in individual networks are canonically represented using low-dimensional vectors, one per gene or protein. These vectors can then be plugged into off-the-shelf machine learning methods to derive functional insights about genes or proteins. We present tools based on Mashup that achieve state-of-the-art performance in three diverse functional inference tasks: protein function prediction, gene ontology reconstruction, and genetic interaction prediction. Mashup enables deeper insights into the structure of rapidly accumulating and diverse biological network data and can be broadly applied to other network science domains.Entities:
Keywords: dimensionality reduction; drug response prediction; gene function prediction; gene ontology reconstruction; genetic interaction prediction; heterogeneous networks; interactome analysis; network diffusion; network integration
Year: 2016 PMID: 27889536 PMCID: PMC5225290 DOI: 10.1016/j.cels.2016.10.017
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304