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Minimizing and quantifying uncertainty in AI-informed decisions: Applications in medicine

  • Samuel D. Curtis
  • , Sambit Panda
  • , Adam Li
  • , Haoyin Xu
  • , Yuxin Bai
  • , Itsuki Ogihara
  • , Eliza O’Reilly
  • , Yuxuan Wang
  • , Lisa Dobbyn
  • , Maria Popoli
  • , Janine Ptak
  • , Nadine Nehme
  • , Natalie Silliman
  • , Jeanne Tie
  • , Peter Gibbs
  • , Lan T. Ho-Pham
  • , Bich N.H. Tran
  • , Thach S. Tran
  • , Tuan V. Nguyen
  • , Ehsan Irajizad
  • Michael Goggins, Christopher L. Wolfgang, Tian Li Wang, Ie Ming Shih, Amanda Fader, Anne Marie Lennon, Ralph H. Hruban, Chetan Bettegowda, Lucy Gilbert, Kenneth W. Kinzler, Nickolas Papadopoulos, Bert Vogelstein*, Joshua T. Vogelstein*, Christopher Douville*
*Corresponding author for this work
  • Johns Hopkins University
  • Columbia University
  • Walter and Eliza Hall Institute of Medical Research
  • University of Melbourne
  • Western Health
  • Pham Ngoc Thach University of Medicine
  • Saigon Precision Medicine Research Center
  • University of Technology Sydney
  • Tâm Anh Research Institute
  • University of New South Wales
  • University of Texas MD Anderson Cancer Center
  • New York University
  • University of Pittsburgh
  • McGill University

Research output: Contribution to journalJournal Article peer-review

1 Scopus citations

Abstract

AI is now a cornerstone of modern dataset analysis. In many real world applications, practitioners are concerned with controlling specific kinds of errors, rather than minimizing the overall number of errors. For example, biomedical screening assays may primarily be concerned with mitigating the number of false positives rather than false negatives. Quantifying uncertainty in AI-based predictions, and in particular those controlling specific kinds of errors, remains theoretically and practically challenging. We develop a strategy called multidimensional informed generalized hypothesis testing (MIGHT) which we prove accurately quantifies uncertainty and confidence given sufficient data, and concomitantly controls for particular error types. Our key insight was that it is possible to integrate canonical cross-validation and parametric calibration procedures within a nonparametric ensemble method. Simulations demonstrate that while typical AI based-approaches cannot be trusted to obtain the truth, MIGHT can be. We apply MIGHT to answer an open question in liquid biopsies using circulating cell-free DNA (ccfDNA) in individuals with or without cancer: Which biomarkers, or combinations thereof, can we trust? Performance estimates produced by MIGHT on ccfDNA data have coefficients of variation that are often orders of magnitude lower than other state of the art algorithms such as support vector machines, random forests, and Transformers, while often also achieving higher sensitivity. We find that combinations of variable sets often decrease rather than increase sensitivity over the optimal single variable set because some variable sets add more noise than signal. This work demonstrates the importance of quantifying uncertainty and confidence—with theoretical guarantees—for the interpretation of real-world data.

Original languageEnglish
Article numbere2424203122
Pages (from-to)e2424203122
JournalProceedings of the National Academy of Sciences of the United States of America
Volume122
Issue number34
DOIs
StatePublished - 26 08 2025
Externally publishedYes

Bibliographical note

Publisher Copyright:
Copyright © 2025 the Author(s). Published by PNAS.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • biomarkers
  • biomedical assays
  • cancer screening
  • hypothesis testing
  • predictive modeling

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