Interpretable AI for inference of causal molecular relationships from omics data

The discovery of molecular relationships from high-dimensional data is a major open problem in bioinformatics. Machine learning and feature attribution models have shown great promise in this context but lack causal interpretation. Here, we show that a popular feature attribution model, under certai...

Full description

Saved in:
Bibliographic Details
Published inScience advances Vol. 11; no. 7; p. eadk0837
Main Authors Dibaeinia, Payam, Ojha, Abhishek, Sinha, Saurabh
Format Journal Article
LanguageEnglish
Published United States 14.02.2025
Subjects
Online AccessGet full text
ISSN2375-2548
2375-2548
DOI10.1126/sciadv.adk0837

Cover

More Information
Summary:The discovery of molecular relationships from high-dimensional data is a major open problem in bioinformatics. Machine learning and feature attribution models have shown great promise in this context but lack causal interpretation. Here, we show that a popular feature attribution model, under certain assumptions, estimates an average of a causal quantity reflecting the direct influence of one variable on another. We leverage this insight to propose a precise definition of a gene regulatory relationship and implement a new tool, CIMLA (Counterfactual Inference by Machine Learning and Attribution Models), to identify differences in gene regulatory networks between biological conditions, a problem that has received great attention in recent years. Using extensive benchmarking on simulated data, we show that CIMLA is more robust to confounding variables and is more accurate than leading methods. Last, we use CIMLA to analyze a previously published single-cell RNA sequencing dataset from subjects with and without Alzheimer’s disease (AD), discovering several potential regulators of AD. A connection is shown between a popular machine learning attribution model and causal molecular relationships in gene networks.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2375-2548
2375-2548
DOI:10.1126/sciadv.adk0837