scholarly journals Accurate and efficient gene function prediction using a multi-bacterial network

Author(s):  
Jeffrey N Law ◽  
Shiv D Kale ◽  
T M Murali

Abstract Motivation Nearly 40% of the genes in sequenced genomes have no experimentally or computationally derived functional annotations. To fill this gap, we seek to develop methods for network-based gene function prediction that can integrate heterogeneous data for multiple species with experimentally based functional annotations and systematically transfer them to newly sequenced organisms on a genome-wide scale. However, the large sizes of such networks pose a challenge for the scalability of current methods. Results We develop a label propagation algorithm called FastSinkSource. By formally bounding its rate of progress, we decrease the running time by a factor of 100 without sacrificing accuracy. We systematically evaluate many approaches to construct multi-species bacterial networks and apply FastSinkSource and other state-of-the-art methods to these networks. We find that the most accurate and efficient approach is to pre-compute annotation scores for species with experimental annotations, and then to transfer them to other organisms. In this manner, FastSinkSource runs in under 3 min for 200 bacterial species. Availability and implementation An implementation of our framework and all data used in this research are available at https://github.com/Murali-group/multi-species-GOA-prediction. Supplementary information Supplementary data are available at Bioinformatics online.

2019 ◽  
Author(s):  
Jeffrey Law ◽  
Shiv Kale ◽  
T. M. Murali

AbstractMotivationNearly 40% of the genes in sequenced genomes have no experimentally- or computationally-derived functional annotations. To fill this gap, we seek to develop methods for network-based gene function prediction that can integrate heterogeneous data for multiple species with experimentally-based functional annotations and systematically transfer them to newly-sequenced organisms on a genomewide scale. However, the large size of such networks pose a challenge for the scalability of current methods.ResultsWe develop a label propagation algorithm called FastSinkSource. By formally bounding its the rate of progress, we decrease the running time by a factor of 100 without sacrificing accuracy. We systematically evaluate many approaches to construct multi-species bacterial networks and apply FastSinkSource and other state-of-the-art methods to these networks. We find that the most accurate and efficient approach is to pre-compute annotation scores for species with experimental annotations, and then to transfer them to other organisms. In this manner, FastSinkSource runs in under three minutes for 200 bacterial species.Availability and ImplementationPython implementations of each algorithm and all data used in this research are available at http://bioinformatics.cs.vt.edu/~jeffl/supplements/[email protected] InformationA supplementary file is available at bioRxiv online.


PLoS ONE ◽  
2010 ◽  
Vol 5 (8) ◽  
pp. e12139 ◽  
Author(s):  
Han Yan ◽  
Kavitha Venkatesan ◽  
John E. Beaver ◽  
Niels Klitgord ◽  
Muhammed A. Yildirim ◽  
...  

2021 ◽  
Author(s):  
Flavio Pazos Obregón ◽  
Diego Silvera ◽  
Pablo Soto ◽  
Patricio Yankilevich ◽  
Gustavo Guerberoff ◽  
...  

Motiviation: The function of most genes is unknown. The best results in gene function prediction are obtained with machine learning-based methods that combine multiple data sources, typically sequence derived features, protein structure and interaction data. Even though there is ample evidence showing that a gene's function is not independent of its location, the few available examples of gene function prediction based on gene location relay on sequence identity between genes of different organisms and are thus subjected to the limitations of the relationship between sequence and function. Results: Here we predict thousands of gene functions in five eukaryotes (Saccharomyces cerevisiae, Caenorhabditis elegans, Drosophila melanogaster, Mus musculus and Homo sapiens) using machine learning models trained with features derived from the location of genes in the genomes to which they belong. To the best of our knowledge this is the first work in which gene function prediction is successfully achieved in eukaryotic genomes using predictive features derived exclusively from the relative location of the genes. Contact: [email protected] Supplementary information: http://gfpml.bnd.edu.uy


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