Abstract

BackgroundThe uncovering of genes linked to human diseases is a pressing challenge in molecular biology and precision medicine. This task is often hindered by the large number of candidate genes and by the heterogeneity of the available information. Computational methods for the prioritization of candidate genes can help to cope with these problems. In particular, kernel-based methods are a powerful resource for the integration of heterogeneous biological knowledge, however, their practical implementation is often precluded by their limited scalability.ResultsWe propose Scuba, a scalable kernel-based method for gene prioritization. It implements a novel multiple kernel learning approach, based on a semi-supervised perspective and on the optimization of the margin distribution. Scuba is optimized to cope with strongly unbalanced settings where known disease genes are few and large scale predictions are required. Importantly, it is able to efficiently deal both with a large amount of candidate genes and with an arbitrary number of data sources. As a direct consequence of scalability, Scuba integrates also a new efficient strategy to select optimal kernel parameters for each data source. We performed cross-validation experiments and simulated a realistic usage setting, showing that Scuba outperforms a wide range of state-of-the-art methods.ConclusionsScuba achieves state-of-the-art performance and has enhanced scalability compared to existing kernel-based approaches for genomic data. This method can be useful to prioritize candidate genes, particularly when their number is large or when input data is highly heterogeneous. The code is freely available at https://github.com/gzampieri/Scuba.

Highlights

  • The uncovering of genes linked to human diseases is a pressing challenge in molecular biology and precision medicine

  • The identification of the genes underlying human diseases is a major goal in current molecular genetics research

  • Unbalanced multiple kernel learning: Scalable Unbalanced gene prioritization (Scuba) In the previous section we introduced Easy multiple kernel learning (EasyMKL), a scalable, efficient kernel integration approach

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Summary

Introduction

The uncovering of genes linked to human diseases is a pressing challenge in molecular biology and precision medicine. This task is often hindered by the large number of candidate genes and by the heterogeneity of the available information. In traditional genotype-phenotype mapping approaches - as Zampieri et al BMC Bioinformatics (2018) 19:23 well as in genome-wide association studies - the first step is the identification of the genomic region(s) wherein the genes of interest lie. Once the candidate region is identified, the genes there residing are prioritized and analysed for the presence of possible causative mutations [1]. In new generation sequencing studies this process is inverted as the first step is the identification of mutations, followed by prioritization and final validation [4]. All of them follow the “guilt-by-association” principle, i.e. disease genes are sought by looking for similarities to genes already associated to the pathology of interest [1]

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