Evidence map›Paper›PMID 41758180›Full record

ArticlePacific Symposium on Biocomputing. Pacific Symposium on Biocomputing2026

DeepDiff-SHAP: Interpretable deep learning for subgroup-specific causal hypothesis generation using conditional SHAP.

Aditya Sriram, Soyeon Kim, Joseph A Carcillo, Hyun Jung Park

Abstract read
In one paragraph

Article in Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Aditya SriramDepartment of Human Genetics, University of Pittsburgh, Pittsburgh, PA, USA.
Soyeon KimDepartment of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.
Joseph A CarcilloDepartment of Pediatrics, University of Pittsburgh, Pittsburgh, PA, USA.
Hyun Jung ParkDepartment of Human Genetics, University of Pittsburgh, Pittsburgh, PA, USA, hyp15@pitt.edu.

Funding

Inflammation Phenotypes in Pediatric Sepsis Induced Multiple Organ Failure RenewalR01GM108618 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOSEPH A CARCILLO · 2014 to 2026
$5.4M
High-Throughput Computing for Genomics and Bioinformatics ResearchS10OD028483 · OD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LEE, ADRIAN V · 2021 to 2021
$574k
NIGMS NIH HHS R01 GM108618NIH HHS S10 OD028483Swiss National Science Foundation 2-4570.5UK Biobank 83829
6 · The paper itself

Abstract

Precision medicine aims to tailor healthcare strategies to individual differences in genetic, clinical, and environmental factors. However, identifying subgroup-specific causal relationships in complex biomedical data remains a major challenge, especially when standard causal inference methods average over population heterogeneity. We introduce DeepDiff-SHAP, a novel framework that combines regression-based and deep learning-based differential causal inference to detect changes in causal relationships across patient subgroups. DeepDiff-SHAP integrates conditional SHapley Additive exPlanations (SHAP) to estimate conditional dependencies and perform nonlinear differential causal inference in a principled, interpretable manner. Applying DeepDiff-SHAP to two population-scale datasets, the CDC Diabetes Health Indicators Dataset and a UK Biobank sepsis cohort stratified by hypertension status, we identified clinically meaningful and subgroupspecific causal changes in relationships between features across the datasets including age, general health, alkaline phosphatase, and cholesterol. Our results reinforce the idea that deep learning enhances sensitivity to complex interaction patterns overlooked by linear models, providing new biological insights into disease progression and comorbidity-specific risk mechanisms. DeepDiff-SHAP offers a scalable and interpretable solution to uncover individualized causal pathways, advancing the goal of truly personalized medicine.

Indexed as

Deep LearningCausalityComputational BiologyHumansHypertensionPrecision MedicineUK Biobank

Identifiers

PMID41758180
PMCPMC13159393

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.