Stable solution to l -based robust inductive matrix completion and its application in linking long noncoding RNAs to human diseases.

Journal: BMC medical genomics
Published Date:

Abstract

BACKGROUNDS: A large number of long intergenic non-coding RNAs (lincRNAs) are linked to a broad spectrum of human diseases. The disease association with many other lincRNAs still remain as puzzle. Validation of such links between the two entities through biological experiments are expensive. However, a plethora lincRNA-data are available now, thanks to the High Throughput Sequencing (HTS) platforms, Genome Wide Association Studies (GWAS), etc, which opens the opportunity for cutting-edge machine learning and data mining approaches to extract meaningful relationships among lincRNAs and diseases. However, there are only a few in silico lincRNA-disease association inference tools available to date, and none of them utilizes side information of both the entities simultaneously in a single framework.

Authors

  • Ashis Kumer Biswas
    Department of Computer Science and Engineering, University of Colorado Denver, Denver, 80204, Colorado, USA.
  • Dongchul Kim
    Department of Computer Science, University of Rio Grande Valley, Edinburg, 78541, Texas, USA.
  • Mingon Kang
    Department of Computer Science, Kennesaw State University, Marietta, 30060, Georgia, USA.
  • Chris Ding
    Department of Computer Science and Engineering, University of Texas at Arlington, Arlington, 76019, Texas, USA.
  • Jean X Gao
    Department of Computer Science and Engineering, University of Texas at Arlington, Arlington, 76019, Texas, USA. gao@uta.edu.