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Adaptive Frontier Exploration on Graphs with Applications to Network-Based Disease Testing

NeurIPS 2025 · Graph learning › Graph algorithms and clustering · approach: Continuous DAG structure learning · 0 citations (OpenAlex)

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Formulates adaptive frontier exploration on graphs (AFEG) as a discounted sequential testing problem and proposes a Gittins-index policy that is provably optimal on forests, with an efficient piecewise-linear implementation and strong empirical results on synthetic and real sexual-contact networks for disease testing.

Problem

Sequentially choosing nodes on a graph with unknown Markov-correlated discrete labels to maximize discounted label-dependent rewards, when actions are restricted to the frontier of previously selected nodes (e.g., network-based disease testing).

Approach

Reduce frontier-constrained AFEG on forests to a discrete branching bandit with history-dependent rewards and compute Gittins indices efficiently via piecewise-linear representations of the recursive phi and Phi functions; on general graphs, apply the same policy to a BFS spanning tree heuristically.

Key results

Measured effects reported in the paper

What was changedWhereMeasuredEffect
use Gittins instead of Random, Greedy, or DQNAFEG policies on synthetic tree graphs · Synthetic treesexpected accumulated discounted rewardHelped
use Gittins instead of Greedy or DQNAFEG policies on synthetic non-tree graphs · Synthetic 50-node graphs with added edgesexpected accumulated discounted rewardMixed
use Gittins instead of other baselinesAFEG policies on real-world sexual interaction graphs · Gonorrhea, Chlamydia, Syphilis, HIV, and Hepatitisfraction of positive cases detectedHelped
use Gittins instead of other baselinesAFEG policies on the HIV interaction graph · HIV, half the population testedfraction of positive cases detected: nearly all vs about 80%Helped
increase noise in the available distribution from QεAFEG policies evaluated using the HIV distribution · HIVfraction of positive cases detectedHurt

Surprising findings

Limitations

Experimental setup

Datasets: ICPSR 22140 sexual interaction network data (Gonorrhea, Chlamydia, Syphilis, HIV, Hepatitis) synthetic random trees

Benchmarks: synthetic trees n=10,50,100 synthetic non-tree graphs ICPSR sexual interaction graphs subsampled to 300 nodes

Metrics: expected accumulated discounted reward fraction of positive cases detected

Baselines: Random Greedy DQN Optimal

Builds on: Gittins index branching bandits adaptive submodularity deep Q-network

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