Machine learning to detect signatures of disease in liquid biopsies - a user's guide.

Journal: Lab on a chip
Published Date:

Abstract

New technologies that measure sparse molecular biomarkers from easily accessible bodily fluids (e.g. blood, urine, and saliva) are revolutionizing disease diagnostics and precision medicine. Microchip devices can measure more disease biomarkers with better sensitivity and specificity each year, but clinical interpretation of these biomarkers remains a challenge. Single biomarkers in 'liquid biopsy' often cannot accurately predict the state of a disease due to heterogeneity in phenotype and disease expression across individuals. To address this challenge, investigators are combining multiplexed measurements of different biomarkers that together define robust signatures for specific disease states. Machine learning is a useful tool to automatically discover and detect these signatures, especially as new technologies output increasing quantities of molecular data. In this paper, we review the state of the field of machine learning applied to molecular diagnostics and provide practical guidance to use this tool effectively and to avoid common pitfalls.

Authors

  • Jina Ko
    Department of Bioengineering, School of Engineering and Applied Sciences, University of Pennsylvania, Philadelphia, Pennsylvania, USA. daveissadore@gmail.com.
  • Steven N Baldassano
  • Po-Ling Loh
  • Konrad Kording
    Laura Prosser, PhD, PTR is a Assistant Professor of Pediatrics, the Perelman School of Medicine, University of Pennsylvania and a physical therapist, Children's Hospital of Philadelphia.
  • Brian Litt
    Penn Center for Neuroengineering and Therapeutics, University of Pennsylvania, Philadelphia, PA, United States of America.
  • David Issadore