Machine learning, the kidney, and genotype-phenotype analysis.

Journal: Kidney international
Published Date:

Abstract

With biomedical research transitioning into data-rich science, machine learning provides a powerful toolkit for extracting knowledge from large-scale biological data sets. The increasing availability of comprehensive kidney omics compendia (transcriptomics, proteomics, metabolomics, and genome sequencing), as well as other data modalities such as electronic health records, digital nephropathology repositories, and radiology renal images, makes machine learning approaches increasingly essential for analyzing human kidney data sets. Here, we discuss how machine learning approaches can be applied to the study of kidney disease, with a particular focus on how they can be used for understanding the relationship between genotype and phenotype.

Authors

  • Rachel S G Sealfon
    Center for Computational Biology, Flatiron Institute, Simons Foundation, New York, New York, USA.
  • Laura H Mariani
    Division of Nephrology, University of Michigan, Ann Arbor, Michigan, USA.
  • Matthias Kretzler
    Division of Nephrology, University of Michigan, Ann Arbor, Michigan, USA. Electronic address: kretzler@umich.edu.
  • Olga G Troyanskaya
    Lewis-Sigler Institute for Integrative Genomics, Princeton University, Princeton, NJ, USA. ogt@cs.princeton.edu.