Your browser doesn't support javascript.
loading
Predicting synthetic lethal interactions using heterogeneous data sources.
Liany, Herty; Jeyasekharan, Anand; Rajan, Vaibhav.
Afiliação
  • Liany H; Department of Computer Science, School of Computing, National University of Singapore, Singapore, Singapore.
  • Jeyasekharan A; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Rajan V; Department of Information Systems and Analytics, School of Computing, National University of Singapore, Singapore, Singapore.
Bioinformatics ; 36(7): 2209-2216, 2020 04 01.
Article em En | MEDLINE | ID: mdl-31782759
ABSTRACT
MOTIVATION A synthetic lethal (SL) interaction is a relationship between two functional entities where the loss of either one of the entities is viable but the loss of both entities is lethal to the cell. Such pairs can be used as drug targets in targeted anticancer therapies, and so, many methods have been developed to identify potential candidate SL pairs. However, these methods use only a subset of available data from multiple platforms, at genomic, epigenomic and transcriptomic levels; and hence are limited in their ability to learn from complex associations in heterogeneous data sources.

RESULTS:

In this article, we develop techniques that can seamlessly integrate multiple heterogeneous data sources to predict SL interactions. Our approach obtains latent representations by collective matrix factorization-based techniques, which in turn are used for prediction through matrix completion. Our experiments, on a variety of biological datasets, illustrate the efficacy and versatility of our approach, that outperforms state-of-the-art methods for predicting SL interactions and can be used with heterogeneous data sources with minimal feature engineering. AVAILABILITY AND IMPLEMENTATION Software available at https//github.com/lianyh. SUPPLEMENTARY INFORMATION Supplementary data are available at Bioinformatics online.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Genômica Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Software / Genômica Idioma: En Ano de publicação: 2020 Tipo de documento: Article