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Whose Behaviour Gets Modelled? ABMs, Data Gaps, and the Risk of Simulating the Easy-to-Reach

Started by Rhoda Nakhosi Oct 19, 2026 3 replies 👁 3 views
Rhoda Nakhosi Admin Community Champion (1,500+ points) Community Champion
Oct 19, 2026 at 11:13 am
@all
A question about what our models quietly leave out: when we build an ABM, whose behaviour actually gets represented and whose doesn't?
ABMs need granular data on individual behaviour, networks, and mobility. But that data isn't evenly available. Some populations are well-documented; others are systematically invisible. People who avoid services, are missed by sampling frames, or live where data infrastructure is weak. The result is a model calibrated on the most reachable, not the most representative.
Three questions:
1. Data driven exclusion. Has anyone built an ABM where a key population had to be left out or approximated because data didn't exist? How did you handle it and did you flag the gap?
2. Whose behaviour is "average"? If the data skews toward certain groups, are we modelling the behaviour of the easy-to-survey as if it were universal?
3. Equity in validation. Should ABMs be assessed not just on accuracy but on whether they represent the populations most affected by the decisions they inform?
I'm curious whether anyone has modelled a population with thin data or whether the honest answer is that some questions shouldn't be modelled until the data catches up.
My view: ABMs can either expose or conceal inequality depending on who's in the data. That should be a deliberate design choice, not an accident of what was available.
Nonvicks Ochieng Member Community Champion (1,500+ points) Community Champion
10 hours ago

@Rhoda Nakhosi This is a critical reflection that touches the heart of modeling ethics and spatial/social justice. You’ve articulated a problem that too often gets buried in the "limitations" section of academic papers rather than driving upfront model design.

Here are perspectives and experiences addressing your three core questions:

1. Data-Driven Exclusion: Handling Missing or Missing-by-Design Populations

Leaving out marginalized or hard-to-reach populations isn't just a data quality issue—it introduces structural bias into model dynamics. When data doesn't exist, modelers typically rely on three primary strategies, each with distinct trade-offs:

  • Synthetic Population Generation & Constraint Matching: Rather than relying purely on empirical survey samples, synthetic micro-data can be generated using marginal distributions (e.g., census aggregates) and spatial micro-simulation. Where individual-level data is thin, Bayesian updating or iterative proportional fitting (IPF) can build plausible agent distributions while explicitly acknowledging missing attributes.

  • Bounding via Scenario Ensembles (Worst-Case / Best-Case Parameters): When exact behavioral parameters for a group are unknown, instead of assigning them "average" behavior, researchers simulate the full parameter space. Running sensitivity analyses across extreme behavioral bounds reveals whether the missing population's behavior creates tipping points or systemic shifts in the outcomes.

  • Participatory Modeling & Qualitative Imputation: Grounding agent rules in qualitative research (focus groups, key informant interviews, expert-elicited heuristics) allows models to represent behaviors that standard quantitative surveys miss (e.g., trust-based informal networks, avoidance of formal services).

How to flag the gap: Transparent documentation via frameworks like ODD+D (Overview, Design Concepts, and Details + Human Decision Making) is essential. Modelers should explicitly document data heritage for every agent archetype, designating agents as Empirically Anchored, Qualitatively Informed, or Stylized/Assumed.

Dr. Magoba Member Expert (800+ points) Expert
9 hours ago

This is a critical issue in agent-based modelling (ABM), particularly in public health research and low- and middle-income countries (LMICs).

When populations are missing from the data, they do not cease to exist; they become invisible in the model. This is especially concerning for marginalized communities, people facing barriers to healthcare, and individuals whose behaviours are poorly captured by routine surveillance systems.

From an epidemiological perspective, I believe three principles are essential:

  1. Make exclusion visible. Where data are unavailable, researchers should explicitly document which populations are underrepresented, distinguish observed behaviours from assumptions, and use sensitivity analyses or alternative scenarios to assess how missing populations could affect the findings.

  2. Challenge the assumption of universal behaviour. The average behaviour observed among accessible participants may not reflect the behaviour of the wider population. Differences in socioeconomic status, healthcare access, geography, stigma, and social networks can fundamentally influence individual decisions and interactions.

  3. Make equity part of validation. An ABM should be assessed not only on its overall predictive accuracy but also on how well it captures outcomes among populations most likely to experience the consequences of policy decisions. A model can perform well on average while systematically misrepresenting vulnerable groups.

Importantly, limited data should not automatically prevent modelling. It should, however, change how confidently we interpret the results. Participatory research, qualitative evidence, transparent assumptions, uncertainty analysis, and targeted data collection can help represent populations for whom granular data are scarce.

My central argument is that data availability should not determine whose experiences count. ABMs should make uncertainty and structural inequality visible rather than inadvertently reproducing them. Equity must be a deliberate component of model design, calibration, validation, and interpretation—not an afterthought.

Charles Member Expert (800+ points) Expert
3 hours ago

Thank you Rhoda Nakhosi for raising this. Very timely question.

From locally led work in Rwanda, this data gap is not theoretical for us.

1. Data driven exclusion: In our youth and community programs, the most affected are often the least documented — youth out of school, informal workers, families not in formal registries. When we build any planning model, we have faced that we must approximate. Our approach has been to not leave them out, but to name the approximation clearly and reduce reliance on only formal data.
2. Whose behaviour is "average"? This is the risk. If we model the easy-to-reach as the average, we plan for the visible community, not the real community. For us, average behaviour from accessible groups often hides differences in mobility, access to information, and trust in services. Assuming universality distorts decisions.
3. Equity in validation: Yes, absolutely. Validation should ask: does this model work for those most affected by the decision? If it is accurate on average but misses the vulnerable, it is not valid for equity decisions.
My view: before we ask if we have enough data to model, we should ask who becomes invisible if we do. In some cases we should pause and invest in better community data first, through local organisations who already have trust.
ABMs should make the invisible visible by design, not by accident.