Datasets:
scenario_id string | inflammation_load float64 | glucose_variability float64 | circadian_disruption float64 | immune_surveillance float64 | mitochondrial_stress float64 | repair_signal_clarity float64 | toxin_pressure float64 | tissue_turnover_pressure float64 | constraint_coupling_score float64 | compensatory_capacity_score float64 | case_type string | label int64 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
TR001 | 0.79 | 0.43 | 0.38 | 0.86 | 0.46 | 0.82 | 0.64 | 0.61 | 0.82 | 0.88 | clean | 0 |
TR002 | 0.62 | 0.58 | 0.55 | 0.47 | 0.63 | 0.43 | 0.5 | 0.57 | 0.73 | 0.45 | clean | 1 |
TR003 | 0.34 | 0.31 | 0.57 | 0.55 | 0.52 | 0.18 | 0.36 | 0.43 | 0.54 | 0.51 | unreadability_threshold | 1 |
TR004 | 0.72 | 0.69 | 0.61 | 0.87 | 0.58 | 0.8 | 0.52 | 0.64 | 0.78 | 0.89 | clean | 0 |
TR005 | 0.49 | 0.52 | 0.48 | 0.44 | 0.59 | 0.36 | 0.47 | 0.52 | 0.76 | 0.39 | clean | 1 |
TR006 | 0.83 | 0.36 | 0.3 | 0.78 | 0.4 | 0.74 | 0.67 | 0.58 | 0.69 | 0.81 | clean | 0 |
TR007 | 0.56 | 0.64 | 0.69 | 0.51 | 0.72 | 0.47 | 0.39 | 0.5 | 0.74 | 0.48 | clean | 1 |
TR008 | 0.68 | 0.72 | 0.45 | 0.84 | 0.48 | 0.77 | 0.42 | 0.6 | 0.81 | 0.86 | clean | 0 |
TR009 | 0.39 | 0.73 | 0.74 | 0.4 | 0.7 | 0.42 | 0.34 | 0.46 | 0.63 | 0.43 | clean | 1 |
TR010 | 0.65 | 0.4 | 0.62 | 0.73 | 0.43 | 0.69 | 0.59 | 0.53 | 0.57 | 0.76 | clean | 0 |
TR011 | 0.45 | 0.49 | 0.52 | 0.58 | 0.65 | 0.16 | 0.45 | 0.55 | 0.49 | 0.54 | unreadability_threshold | 1 |
TR012 | 0.78 | 0.7 | 0.63 | 0.88 | 0.56 | 0.83 | 0.6 | 0.67 | 0.84 | 0.91 | clean | 0 |
TR013 | 0.53 | 0.57 | 0.44 | 0.42 | 0.68 | 0.4 | 0.58 | 0.62 | 0.75 | 0.41 | clean | 1 |
TR014 | 0.85 | 0.59 | 0.37 | 0.81 | 0.5 | 0.78 | 0.63 | 0.7 | 0.71 | 0.84 | clean | 0 |
TR015 | 0.42 | 0.68 | 0.8 | 0.47 | 0.74 | 0.39 | 0.3 | 0.41 | 0.66 | 0.44 | clean | 1 |
TR016 | 0.74 | 0.46 | 0.35 | 0.7 | 0.55 | 0.67 | 0.72 | 0.65 | 0.58 | 0.73 | clean | 0 |
TR017 | 0.59 | 0.62 | 0.6 | 0.49 | 0.58 | 0.45 | 0.52 | 0.55 | 0.72 | 0.46 | clean | 1 |
TR018 | 0.67 | 0.73 | 0.58 | 0.85 | 0.62 | 0.76 | 0.49 | 0.63 | 0.79 | 0.87 | clean | 0 |
TR019 | 0.37 | 0.42 | 0.79 | 0.43 | 0.71 | 0.19 | 0.37 | 0.49 | 0.52 | 0.47 | unreadability_threshold | 1 |
TR020 | 0.8 | 0.37 | 0.42 | 0.83 | 0.46 | 0.79 | 0.7 | 0.59 | 0.68 | 0.83 | clean | 0 |
TR021 | 0.58 | 0.55 | 0.5 | 0.46 | 0.67 | 0.37 | 0.54 | 0.61 | 0.77 | 0.4 | clean | 1 |
TR022 | 0.72 | 0.65 | 0.7 | 0.87 | 0.59 | 0.82 | 0.47 | 0.66 | 0.83 | 0.9 | clean | 0 |
TR023 | 0.43 | 0.63 | 0.74 | 0.48 | 0.76 | 0.43 | 0.33 | 0.44 | 0.65 | 0.45 | clean | 1 |
TR024 | 0.87 | 0.5 | 0.34 | 0.8 | 0.53 | 0.73 | 0.74 | 0.69 | 0.74 | 0.85 | clean | 0 |
TR025 | 0.54 | 0.6 | 0.56 | 0.44 | 0.64 | 0.38 | 0.51 | 0.58 | 0.78 | 0.42 | clean | 1 |
TR026 | 0.76 | 0.71 | 0.62 | 0.89 | 0.61 | 0.84 | 0.58 | 0.68 | 0.86 | 0.92 | clean | 0 |
TR027 | 0.36 | 0.39 | 0.83 | 0.5 | 0.79 | 0.17 | 0.35 | 0.45 | 0.55 | 0.5 | unreadability_threshold | 1 |
TR028 | 0.83 | 0.56 | 0.41 | 0.86 | 0.47 | 0.81 | 0.66 | 0.71 | 0.8 | 0.88 | clean | 0 |
TR029 | 0.5 | 0.54 | 0.59 | 0.45 | 0.69 | 0.39 | 0.56 | 0.6 | 0.76 | 0.41 | clean | 1 |
TR030 | 0.69 | 0.74 | 0.53 | 0.85 | 0.57 | 0.77 | 0.45 | 0.61 | 0.7 | 0.84 | clean | 0 |
TR031 | 0.57 | 0.52 | 0.49 | 0.52 | 0.61 | 0.11 | 0.45 | 0.54 | 0.71 | 0.79 | unreadability_threshold | 1 |
TR032 | 0.69 | 0.63 | 0.58 | 0.94 | 0.66 | 0.77 | 0.61 | 0.68 | 0.74 | 0.48 | immune_dominant | 0 |
TR033 | 0.46 | 0.59 | 0.76 | 0.57 | 0.72 | 0.14 | 0.39 | 0.47 | 0.62 | 0.82 | unreadability_threshold | 1 |
TR034 | 0.73 | 0.71 | 0.67 | 0.91 | 0.69 | 0.74 | 0.66 | 0.72 | 0.79 | 0.52 | immune_dominant | 0 |
TR035 | 0.51 | 0.48 | 0.55 | 0.49 | 0.58 | 0.13 | 0.42 | 0.5 | 0.56 | 0.76 | unreadability_threshold | 1 |
TR036 | 0.77 | 0.68 | 0.6 | 0.93 | 0.64 | 0.8 | 0.7 | 0.74 | 0.81 | 0.55 | immune_dominant | 0 |
What this dataset does
This dataset tests whether a model can detect pre-cancer instability from constraint geometry rather than single-variable thresholds.
The task is not cancer diagnosis.
The task is to classify whether a synthetic tissue ecology has crossed into a persistent instability transition.
Core Stability Idea
The dataset represents a stability-transition hypothesis.
Cancer vulnerability may begin when tissue regulation loses self-correcting coherence before visible disease appears.
The positive class does not indicate cancer.
It indicates that the tissue ecology has entered a persistent instability regime.
Prediction Target
label = 1
The tissue-state scenario has crossed into persistent instability transition.
label = 0
The tissue-state scenario remains compensated despite stress.
Row Structure
Each row represents a synthetic tissue-state scenario.
Columns:
- scenario_id
- inflammation_load
- glucose_variability
- circadian_disruption
- immune_surveillance
- mitochondrial_stress
- repair_signal_clarity
- toxin_pressure
- tissue_turnover_pressure
- constraint_coupling_score
- compensatory_capacity_score
- case_type
- label
Case Types
clean
Standard stability geometry cases.
Instability emerges through the interaction of coupled pressure and compensation limits.
Examples include:
- High coupling plus weak compensation leads to instability.
- High coupling plus strong compensation remains stable.
unreadability_threshold
Repair signal clarity falls below a critical readability boundary.
These rows represent the hypothesis that instability may emerge from loss of signal interpretation before visible pathology appears.
In these cases:
- Coupling may be moderate.
- Compensation may appear strong.
- Instability emerges because repair readability has collapsed.
immune_dominant
Immune surveillance remains sufficiently strong to preserve stability despite reduced compensatory capacity.
These rows prevent compensation metrics from becoming deterministic predictors.
In these cases:
- Coupling may be high.
- Compensation may appear weak.
- Stability is maintained through immune dominance.
Anti-Shortcut Design
This dataset contains adversarial boundary cases designed to prevent simple threshold-based solutions.
High constraint coupling does not always imply instability.
High compensatory capacity does not always imply stability.
Low compensatory capacity does not always imply instability.
Low inflammation does not always imply stability.
High inflammation does not always imply instability.
Repair signal clarity can override the apparent reserve profile when it collapses below a critical readability boundary.
Immune surveillance can override apparent reserve weakness when sufficiently strong.
The benchmark is designed so that models must learn interactions rather than individual-variable thresholds.
Evaluation
Submit predictions in the format:
scenario_id,prediction
Run:
python scorer.py predictions.csv data/test.csv
The scorer returns:
- accuracy
- precision
- recall
- f1
- confusion_matrix
- accuracy_clean
- accuracy_unreadability_threshold
- accuracy_immune_dominant
- case_type_accuracy_macro
Scorer Design
The scorer automatically discovers case types from the test set.
It does not rely on a hardcoded list of pathway categories.
Any case type present in the evaluation set automatically receives its own accuracy metric.
This allows the benchmark to evolve without requiring scorer modifications.
Future dataset versions may introduce additional pathway categories such as:
- compensation_exhaustion
- inflammatory_lock_in
- repair_recovery
- metabolic_instability
- immune_escape
The scorer will automatically generate:
- accuracy_
for every case type present in the test set.
This makes the evaluation framework extensible while preserving compatibility across dataset versions.
In addition to overall accuracy, the scorer reports pathway-specific accuracies so researchers can identify which stability-transition mechanisms a model understands and which mechanisms remain failure modes.
Macro Case-Type Accuracy
case_type_accuracy_macro is the unweighted mean of accuracy across case types.
Each pathway receives equal weight regardless of how many rows belong to that pathway.
This prevents dominant case types from masking poor performance on rarer but theoretically important pathways such as unreadability_threshold.
Structural Contribution
Most oncology datasets attempt to predict disease presence.
This dataset attempts to predict stability transition.
The benchmark explicitly represents multiple pathways into instability:
- Coupling-driven instability
- Unreadability-driven instability
- Immune-dominant stabilization
A successful model cannot rely on a single marker.
It must infer the interaction geometry that generates the transition boundary.
Structural Note
This dataset is synthetic.
It is designed to evaluate structural reasoning rather than provide medical diagnosis.
The generator logic is intentionally withheld.
The purpose is to evaluate whether a model can infer instability geometry from interacting constraints rather than relying on simple correlations.
License
MIT
- Downloads last month
- 22