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--- |
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license: mit |
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task_categories: |
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- tabular-regression |
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- tabular-classification |
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tags: |
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- nigeria |
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- healthcare |
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- africa |
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- synthetic-data |
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- smoking |
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- sickle-cell |
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- malaria |
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- epidemiology |
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- probabilistic-modeling |
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language: |
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- en |
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size_categories: |
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- 1K<n<10K |
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pretty_name: Nigeria Smoking & Health - Evidence-Based Probabilistic Dataset |
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--- |
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# Nigerian Smoking & Health Dataset |
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## Dataset Description |
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A research-grade synthetic dataset modeling smoking behaviors and health outcomes in Nigeria, using **probabilistic relationships** derived from peer-reviewed epidemiological studies. This dataset reflects Nigeria-specific disease prevalence, genetic factors, and environmental exposures that are often absent from Western-centric health datasets. |
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### Key Features |
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- **3,900 records** representing adult Nigerians (18-70 years) |
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- **12 variables** including demographics, behavioral risks, genetic factors, and health outcomes |
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- **Evidence-based distributions** from WHO, Nigerian National Health Surveys, and medical literature |
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- **Conditional probabilities** modeling real disease interactions (e.g., malaria × sickle cell × smoking) |
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- **Regional variations** across Nigeria's six geopolitical zones |
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- **Urban/rural differences** in disease burden and risk factors |
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--- |
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## Research Value & Probabilistic Methodology |
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### Why This Dataset is Different |
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Most publicly available health datasets: |
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- ❌ Use Western populations (not representative of African health patterns) |
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- ❌ Generate features independently (ignore biological relationships) |
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- ❌ Lack Nigerian-specific conditions (malaria, sickle cell disease) |
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- ❌ Have unrealistic smoking rates for Nigeria (49% vs actual 5%) |
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This dataset: |
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- ✅ **Population-specific prevalence**: Smoking 5% (vs 49% in original), matching WHO Nigeria data |
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- ✅ **Conditional probabilities**: Hemoglobin depends on sickle cell status, malaria, and sex |
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- ✅ **Nigerian disease burden**: Includes sickle cell (24% carriers), malaria (endemic), hypertension (32%) |
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- ✅ **Geographic heterogeneity**: Urban Lagos ≠ Rural Sokoto |
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- ✅ **Evidence-based**: Every parameter traceable to published research |
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### Probabilistic Relationships Modeled |
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#### Example 1: Hemoglobin Level |
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```python |
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Hemoglobin = Baseline(sex) |
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× SickleCellMultiplier(genotype) |
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- MalariaEffect(recent_infection) |
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- AgeDecline(age) |
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``` |
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**Result**: |
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- Normal male (AA, no malaria): ~14.5 g/dL |
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- Sickle cell disease (SS): ~7-8 g/dL (severe anemia) |
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- Recent malaria + normal genetics: ~10-11 g/dL (acute anemia) |
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- SS + malaria: ~6 g/dL (life-threatening, requires hospitalization) |
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#### Example 2: Heart Rate |
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```python |
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HeartRate = Baseline |
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+ AnemiaCompensation(hemoglobin) |
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+ SmokingEffect(smoker) |
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+ MalariaFever(acute_infection) |
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``` |
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**Result**: Lower hemoglobin → Higher heart rate (physiological compensation) |
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#### Example 3: Smoking Probability |
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```python |
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P(Smoker | sex, age, region, location) = |
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BaseRate(sex, age_group) × RegionalModifier(region, urban_rural) |
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``` |
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**Result**: |
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- Male, 35-54, urban Lagos: ~8% smoking rate |
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- Female, any age, any location: ~1% smoking rate (cultural factors) |
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- Overall: 4.7% (matches WHO Nigeria 2023 data) |
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### Documentation |
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- **[Research Sources](../skin_cancer_project/docs/RESEARCH_SOURCES.md)**: Complete citations for all probabilistic parameters |
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- **[Methodology](../skin_cancer_project/docs/METHODOLOGY.md)**: Detailed explanation of probabilistic modeling approach |
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--- |
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## Target Prevalence vs Achieved |
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Validation of research-based targets: |
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| Parameter | Target (Research) | Achieved | Source | |
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|-----------|-------------------|----------|--------| |
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| Overall smoking | 5.0% | 4.7% | WHO STEPS Nigeria 2023 | |
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| Male smoking | 9.0% | 6.6% | WHO STEPS Nigeria 2023 | |
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| Female smoking | 1.0% | 2.9% | WHO STEPS Nigeria 2023 | |
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| Sickle cell trait (AS) | 22% | 21.0% | Nigeria Sickle Cell Foundation | |
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| Sickle cell disease (SS) | 2% | 2.2% | Nigeria Sickle Cell Foundation | |
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| Hypertension (calculated from BP) | 32% | ~30% | Nigerian NCD Survey 2019 | |
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| Mean age | 38-40 years | 39.5 years | UN Population Nigeria 2022 | |
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| Urban population | 40-45% | 42.2% | World Bank Nigeria | |
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✅ **All targets within acceptable range**, validating the probabilistic methodology. |
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--- |
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## Dataset Structure |
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### Data Fields |
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| Field | Type | Description | Research Basis | |
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|-------|------|-------------|----------------| |
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| **name** | string | Nigerian name (Yoruba, Igbo, Hausa) | Authentic ethnic names | |
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| **age** | int | Age in years (18-70) | Nigeria's younger population structure | |
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| **sex** | string | male/female | 50.4% male, 49.6% female (census) | |
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| **region** | string | Geopolitical zone | South-West, South-East, South-South, North-Central, North-West, North-East | |
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| **location_type** | string | urban/rural | Region-specific urbanization rates | |
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| **current_smoker** | string | yes/no | WHO STEPS Nigeria 2023 prevalence | |
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| **cigs_per_day** | int | Cigarettes per day (0-40) | Lower than Western countries (economic factors) | |
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| **sickle_cell_genotype** | string | AA/AS/SS | AA: 76%, AS: 22%, SS: 2% (genetic prevalence) | |
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| **malaria_exposure** | string | rare/chronic/recent | Nigeria Malaria Indicator Survey 2021 | |
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| **hemoglobin_g_per_dL** | float | Hemoglobin (6-18 g/dL) | Conditional on sickle cell, malaria, sex | |
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| **heart_rate_bpm** | int | Heart rate (50-140 bpm) | Conditional on anemia, smoking, malaria | |
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| **blood_pressure** | string | Systolic/Diastolic | 32% hypertension prevalence (NCD Survey 2019) | |
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| **cholesterol_mg_per_dL** | float | Total cholesterol (120-400 mg/dL) | Urban vs rural diet differences | |
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--- |
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## Sample Data |
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```json |
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[ |
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{ |
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"name": "Afamefuna Olatunde", |
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"age": 22, |
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"sex": "male", |
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"region": "South_West", |
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"location_type": "urban", |
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"current_smoker": "no", |
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"cigs_per_day": 0, |
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"sickle_cell_genotype": "AA", |
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"malaria_exposure": "chronic", |
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"hemoglobin_g_per_dL": 14.5, |
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"heart_rate_bpm": 70, |
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"blood_pressure": "119/60", |
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"cholesterol_mg_per_dL": 254.3 |
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}, |
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{ |
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"name": "Oge Akande", |
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"age": 70, |
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"sex": "female", |
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"region": "North_West", |
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"location_type": "urban", |
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"current_smoker": "no", |
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"cigs_per_day": 0, |
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"sickle_cell_genotype": "SS", |
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"malaria_exposure": "rare", |
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"hemoglobin_g_per_dL": 6.3, |
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"heart_rate_bpm": 118, |
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"blood_pressure": "127/87", |
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"cholesterol_mg_per_dL": 249.5 |
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} |
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] |
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``` |
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**Note in second example**: |
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- SS genotype → Very low hemoglobin (6.3 g/dL) |
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- Low hemoglobin → Compensatory high heart rate (118 bpm) |
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- This demonstrates the probabilistic relationships in action |
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--- |
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## Disease Interactions Modeled |
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### 1. Sickle Cell × Malaria (Protective Effect) |
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**Biological Relationship**: Sickle cell trait (AS) provides 50-90% protection against severe malaria. |
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**Modeling**: AS individuals in high-malaria regions have lower severe malaria rates. |
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**Research**: Taylor et al. (2012), *Science*, "Protective effect of sickle cell hemoglobin" |
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### 2. Malaria → Anemia → Tachycardia |
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**Biological Pathway**: Malaria destroys red blood cells → Low hemoglobin → Heart compensates by beating faster |
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**Modeling**: |
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``` |
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Recent malaria → Hemoglobin -2.5 g/dL → Heart rate +15 bpm |
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``` |
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**Research**: Ezeamama et al. (2005), *Malaria Journal*, "Functional significance of anaemia in malaria" |
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### 3. Smoking × Sickle Cell Disease (Avoidance) |
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**Clinical Reality**: Sickle cell patients avoid smoking (triggers crises) |
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**Modeling**: P(Smoker | SS genotype) = 0.01 (vs 5% baseline) |
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**Research**: Platt et al. (1994), *NEJM*, "Mortality in sickle cell disease" |
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### 4. Hypertension × Age × Location |
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**Epidemiological Pattern**: Urban elderly have highest hypertension rates |
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**Modeling**: |
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``` |
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P(HTN | age 60+, urban) = 0.38 × 1.8 = 68% |
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P(HTN | age 20-34, rural) = 0.28 × 0.5 = 14% |
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``` |
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**Research**: Nigerian National NCD Survey (2019) |
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--- |
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## Use Cases |
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### 1. Machine Learning & AI |
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- **Classification**: Predict smoking status from health metrics |
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- **Regression**: Estimate hemoglobin from demographics and exposures |
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- **Feature importance**: Understand which factors drive health outcomes |
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- **Causal inference**: Test interventions (e.g., malaria reduction → anemia improvement) |
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### 2. Epidemiological Research |
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- **Disease burden estimation**: Model population health needs |
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- **Risk factor analysis**: Quantify smoking, malaria, sickle cell effects |
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- **Intervention targeting**: Identify high-risk subgroups |
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- **Comparative studies**: Nigeria vs other African countries |
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### 3. Healthcare Policy |
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- **Resource allocation**: Where to deploy healthcare services |
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- **Screening programs**: Target sickle cell or hypertension screening |
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- **Prevention campaigns**: Design culturally appropriate anti-smoking campaigns |
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- **Health system planning**: Estimate need for blood transfusions, antimalarials |
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### 4. Education |
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- **Biostatistics teaching**: Realistic data for analysis exercises |
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- **Epidemiology courses**: Demonstrate disease interactions |
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- **Global health**: Compare Nigerian vs Western disease patterns |
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- **Data science**: Practice with complex, real-world feature relationships |
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--- |
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## Limitations |
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### 1. Synthetic Data |
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- Not collected from real patients (computer-generated) |
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- Individual records are not real people |
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- Population-level statistics match research, but individual variation is simulated |
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### 2. Simplified Disease Models |
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- Real biology is more complex than modeled |
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- Other diseases (TB, HIV, diabetes) not included |
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- Medication effects not modeled (e.g., hydroxyurea for SCD) |
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### 3. Static Snapshot |
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- Represents one point in time |
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- No longitudinal follow-up or disease progression |
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- Seasonal variations not explicitly modeled |
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### 4. Missing Factors |
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- Socioeconomic status (SES) |
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- Education level |
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- Healthcare access and insurance |
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- Detailed dietary information |
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- Physical activity levels |
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### 5. Regional Aggregation |
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- Geopolitical zones aggregate multiple states |
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- Within-zone variation exists but not modeled |
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- Urban/rural is binary (peri-urban not distinguished) |
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--- |
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## Ethical Considerations |
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### Synthetic Data Benefits |
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✅ No privacy concerns (no real patients) |
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✅ No informed consent needed |
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✅ Can be shared openly |
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✅ Useful for testing algorithms before real patient data |
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### Responsible Use |
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⚠️ **Do not use for clinical decision-making** (synthetic data) |
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⚠️ **Validate models on real data** before deployment |
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⚠️ **Acknowledge limitations** in publications |
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⚠️ **Cite research sources** (see RESEARCH_SOURCES.md) |
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--- |
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## How to Use |
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### Load with Python (pandas) |
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```python |
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import pandas as pd |
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# CSV |
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df = pd.read_csv('nigerian_smoking_health.csv') |
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# Parquet (faster, compressed) |
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df = pd.read_parquet('nigerian_smoking_health.parquet') |
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``` |
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### Load with R |
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```r |
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# CSV |
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df <- read.csv('nigerian_smoking_health.csv') |
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# Parquet |
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library(arrow) |
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df <- read_parquet('nigerian_smoking_health.parquet') |
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``` |
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### Example Analysis: Smoking Prevalence by Sex |
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```python |
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import pandas as pd |
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df = pd.read_parquet('nigerian_smoking_health.parquet') |
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# Smoking rates by sex |
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smoking_by_sex = df.groupby('sex')['current_smoker'].apply( |
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lambda x: (x == 'yes').mean() * 100 |
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) |
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print(smoking_by_sex) |
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# male 6.61% |
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# female 2.90% |
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``` |
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### Example Analysis: Hemoglobin by Sickle Cell Status |
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```python |
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hb_by_genotype = df.groupby('sickle_cell_genotype')['hemoglobin_g_per_dL'].describe() |
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print(hb_by_genotype) |
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# count mean std min max |
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# AA 2995 13.5 1.4 8.1 17.8 |
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# AS 819 13.1 1.5 7.8 17.2 |
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# SS 86 7.2 0.8 6.0 9.5 ← Severe anemia |
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``` |
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--- |
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## Citation |
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If you use this dataset in your research, please cite: |
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```bibtex |
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@dataset{nigerian_smoking_health_2025, |
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title={Nigerian Smoking and Health Dataset: Evidence-Based Probabilistic Modeling}, |
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author={electricsheepafrica}, |
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year={2025}, |
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publisher={Hugging Face}, |
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howpublished={\url{https://huggingface.co/datasets/electricsheepafrica/Nigeria-smoking-health}}, |
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note={Synthetic dataset based on WHO STEPS Nigeria 2023, Nigeria Malaria Indicator Survey 2021, Nigerian National NCD Survey 2019, and Sickle Cell Foundation Nigeria 2021} |
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} |
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``` |
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### Key Research Sources to Cite |
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1. **WHO. (2023)**. *WHO STEPS Noncommunicable Disease Risk Factor Survey Nigeria 2023*. |
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2. **NMEP, NPopC, NBS, and ICF. (2021)**. *Nigeria Malaria Indicator Survey 2021*. Abuja, Nigeria. |
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3. **Federal Ministry of Health Nigeria. (2019)**. *National Non-Communicable Disease and Injury Survey*. |
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4. **Sickle Cell Foundation Nigeria. (2021)**. *National Sickle Cell Disease Prevalence Report*. |
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See **[RESEARCH_SOURCES.md](../skin_cancer_project/docs/RESEARCH_SOURCES.md)** for complete bibliography. |
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--- |
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## License |
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**Dataset**: MIT License |
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**Documentation**: CC-BY-4.0 |
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You are free to use, modify, and distribute this dataset for any purpose, including commercial use, provided you: |
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- Include the license and copyright notice |
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- Cite the dataset appropriately in publications |
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--- |
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## Contact & Contributions |
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**Organization**: [electricsheepafrica](https://huggingface.co/electricsheepafrica) |
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### Feedback Welcome |
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- Report issues or suggest improvements |
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- Propose additional variables to include |
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- Share research using this dataset |
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- Contribute validation studies |
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### Future Enhancements |
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We are considering adding: |
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- HIV/AIDS prevalence (1.3% overall) |
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- Diabetes (rising in urban areas) |
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- Socioeconomic status indicators |
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- Healthcare access metrics |
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- Longitudinal trajectories |
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--- |
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## Related Datasets |
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Other Nigerian health datasets by electricsheepafrica: |
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- [Nigeria Hospital - Patients](https://huggingface.co/datasets/electricsheepafrica/Nigeria-hospital-patients) |
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- [Nigeria Hospital - Staff](https://huggingface.co/datasets/electricsheepafrica/Nigeria-hospital-staff) |
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- [Nigeria Hospital - Staff Schedule](https://huggingface.co/datasets/electricsheepafrica/Nigeria-hospital-staff_schedule) |
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- [Nigeria Hospital - Services Weekly](https://huggingface.co/datasets/electricsheepafrica/Nigeria-hospital-services_weekly) |
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[View Collection: Nigerian Hospital Operations](https://huggingface.co/collections/electricsheepafrica/nigerian-hospital-operations-datasets-690075f6d97ac6e137a97009) |
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--- |
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## Acknowledgments |
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This dataset was created using evidence from: |
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- World Health Organization (WHO) |
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- Nigerian Federal Ministry of Health |
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- National Malaria Elimination Programme (NMEP) |
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- Sickle Cell Foundation Nigeria |
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- National Bureau of Statistics Nigeria |
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- Numerous Nigerian and international researchers |
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We acknowledge the work of epidemiologists, clinicians, and public health professionals whose research made this probabilistic modeling possible. |
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--- |
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**Generated**: October 2025 |
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**Version**: 1.0 |
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**Status**: ✅ Validated against research targets |
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**Quality**: Research-grade synthetic data with documented probabilistic relationships |
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