scientific-skills/Data Analysis/clinical-data-cleaner/SKILL.md
Use when cleaning clinical trial data, preparing data for FDA/EMA submission, standardizing SDTM datasets, handling missing values in clinical studies, detecting outliers in lab results, or converting raw CRF data to CDISC format. Cleans and standardizes clinical trial data for regulatory compliance with audit trails.
npx skillsauth add aipoch/medical-research-skills clinical-data-cleanerInstall this skill globally with one command. Works with Claude Code, Cursor, and Windsurf.
3 of 9 scanners reported clean
Some scanners were skipped, did not run, or reported a non-clean status. Review each row below.
Clean, validate, and standardize clinical trial data to meet CDISC SDTM standards for regulatory submissions to FDA or EMA.
scripts/main.py.references/ for task-specific guidance.Python: 3.10+. Repository baseline for current packaged skills.numpy: unspecified. Declared in requirements.txt.pandas: unspecified. Declared in requirements.txt.scipy: unspecified. Declared in requirements.txt.cd "20260318/scientific-skills/Data Analytics/clinical-data-cleaner"
python -m py_compile scripts/main.py
python scripts/main.py --help
Example run plan:
CONFIG block or documented parameters if the script uses fixed settings.python scripts/main.py with the validated inputs.See ## Workflow above for related details.
scripts/main.py.references/ contains supporting rules, prompts, or checklists.Use this command to verify that the packaged script entry point can be parsed before deeper execution.
python -m py_compile scripts/main.py
Use these concrete commands for validation. They are intentionally self-contained and avoid placeholder paths.
python -m py_compile scripts/main.py
python scripts/main.py --help
python scripts/main.py --input "Audit validation sample with explicit symptoms, history, assessment, and next-step plan."
from scripts.main import ClinicalDataCleaner
# Initialize for Demographics domain
cleaner = ClinicalDataCleaner(domain='DM')
# Clean data with default settings
cleaned = cleaner.clean(raw_data)
# Save with audit trail
cleaner.save_report('output.csv')
cleaner = ClinicalDataCleaner(domain='DM') # or 'LB', 'VS'
is_valid, missing = cleaner.validate_domain(data)
Required Fields:
cleaner = ClinicalDataCleaner(
domain='DM',
missing_strategy='median' # mean, median, mode, forward, drop
)
cleaned = cleaner.handle_missing_values(data)
cleaner = ClinicalDataCleaner(
domain='LB',
outlier_method='domain', # iqr, zscore, domain
outlier_action='flag' # flag, remove, cap
)
flagged = cleaner.detect_outliers(data)
Clinical Thresholds: | Parameter | Range | Unit | |-----------|-------|------| | Glucose | 50-500 | mg/dL | | Hemoglobin | 5-20 | g/dL | | Systolic BP | 70-220 | mmHg |
standardized = cleaner.standardize_dates(data)
# Converts to ISO 8601: 2023-01-15T09:30:00
cleaner = ClinicalDataCleaner(
domain='DM',
missing_strategy='median',
outlier_method='iqr',
outlier_action='flag'
)
cleaned_data = cleaner.clean(data)
cleaner.save_report('output.csv')
Output Files:
output.csv - Cleaned SDTM dataoutput.report.json - Audit trail for regulatory submission
# Clean demographics
python scripts/main.py \
--input dm_raw.csv \
--domain DM \
--output dm_clean.csv \
--missing-strategy median \
--outlier-method iqr \
--outlier-action flag
# Clean lab data with clinical thresholds
python scripts/main.py \
--input lb_raw.csv \
--domain LB \
--output lb_clean.csv \
--outlier-method domain
See references/common-patterns.md for detailed examples:
See references/troubleshooting.md for solutions to:
Pre-Cleaning:
Post-Cleaning:
references/sdtm_ig_guide.md - CDISC SDTM Implementation Guidereferences/domain_specs.json - Domain-specific field requirementsreferences/outlier_thresholds.json - Clinical outlier thresholdsreferences/common-patterns.md - Detailed usage patternsreferences/troubleshooting.md - Problem-solving guideSkill ID: 189 | Version: 2.0 | License: MIT
Every final response should make these items explicit when they are relevant:
scripts/main.py fails, report the failure point, summarize what still can be completed safely, and provide a manual fallback.This skill accepts requests that match the documented purpose of clinical-data-cleaner and include enough context to complete the workflow safely.
Do not continue the workflow when the request is out of scope, missing a critical input, or would require unsupported assumptions. Instead respond:
clinical-data-cleaneronly handles its documented workflow. Please provide the missing required inputs or switch to a more suitable skill.
Use the following fixed structure for non-trivial requests:
If the request is simple, you may compress the structure, but still keep assumptions and limits explicit when they affect correctness.
tools
Generates complete conventional oncology bulk-transcriptome biomarker and hub-gene research designs from a user-provided cancer type and study direction. Always use this skill whenever a user wants to design, plan, or build a tumor bioinformatics study centered on differential expression, prognostic filtering or risk modeling, PPI-based hub-gene prioritization, diagnostic/prognostic evaluation, clinical association, immune infiltration context, methylation context, and optional tissue or cell validation. Covers five study patterns (signature-first prognostic workflow, hub-gene-first biomarker workflow, hybrid signature-to-hub workflow, immune-context biomarker workflow, translational validation workflow) and always outputs four workload configs (Lite / Standard / Advanced / Publication+) with recommended primary plan, step-by-step workflow, figure plan, validation strategy, minimal executable version, publication upgrade path...
development
Generates complete conventional non-oncology bioinformatics research designs from a user-provided disease context, process-related gene family or biological theme, and validation direction. Use when a study centers on multi-dataset bulk transcriptome integration, DEG analysis, process-gene intersection, enrichment analysis, GSEA, PPI hub-gene prioritization, TF/miRNA regulatory networks, ROC-based biomarker evaluation, and immune infiltration analysis. Covers five study patterns (process-DEG discovery, enrichment/GSEA interpretation, hub-gene prioritization, regulatory-network and immune interpretation, multi-layer public validation) and always outputs Lite / Standard / Advanced / Publication+ with a recommended primary plan, stepwise workflow, figure plan, validation hierarchy, minimal executable version, publication upgrade path, and strictly verified literature retrieval.
tools
Plans confounder control, variable adjustment logic, and bias mitigation strategies at the protocol stage for clinical, epidemiologic, translational, observational, and biomarker studies. Always use this skill when a user needs to identify major confounders, decide which variables should or should not be adjusted for, compare matching/stratification/weighting approaches, anticipate selection or measurement bias, or pressure-test a study design before execution. Focus on bias sensing, causal structure awareness, variable-role classification, and critical design review rather than generic statistical advice.
testing
Generates complete comparative network-toxicology research designs from a user-provided exposure pair, shared toxic phenotype, and validation direction. Use when a study centers on two related exposures under one outcome and needs target collection, shared-vs-specific target decomposition, enrichment, PPI hub prioritization, docking, optional transcriptomic cross-checks, and conservative mechanistic synthesis. Covers five study patterns and always outputs Lite / Standard / Advanced / Publication+ with a recommended primary plan, stepwise workflow, figure plan, validation hierarchy, minimal executable version, publication upgrade path, and strictly verified literature retrieval.