Bio Stats Ml Reporting

Bio Stats ML Reporting

Aggregate results, train ML models, and produce reports with validated references.

Instructions

Tool guides and versions: docs/README.md.

1. Join outputs in DuckDB v1.1+ and build feature tables. Arrow / DuckLake integration is the recommended bridge into ML pipelines for large datasets.
2. Train baseline models and evaluate with cross-validation.
   • CPU baseline: scikit-learn v1.5+ for linear/tree/clustering baselines; XGBoost v2.1.4+ for gradient boosting.
   • GPU node available (CUDA): set device="cuda" on XGBoost (native since v2.0) by default. For sklearn-compatible estimators (random forest, k-means, PCA, UMAP), use RAPIDS cuML as a drop-in replacement and record the device in the run log.
3. Generate reports and validate references.
   • Validate the prediction table with scripts/validate_predictions.py. Keep group identifiers and confounder labels in the table so the gate can detect sample/group leakage, class imbalance, calibration failure, batch-outcome imbalance, and performance that does not beat the majority-class null.
4. For exploratory omics projects, aggregate discovery evidence across the literature-derived analysis playbook, annotation, phylogenomics, viromics, and comparative-genomics outputs.
5. Comparative-axes rollup — join the per-axis comparison artifacts produced by upstream skills into a single comparative_axes_summary.tsv. The rollup must have one row per (query genome, axis) and include:
   • genome-property frontier (size, gene count, etc. — link to relative_genome_metrics.tsv and genome_size_frontier.tsv)
   • marker-gene census (link to marker_census.tsv)
   • family copy-number expansions/contractions (link to family_copy_number_comparison.tsv and family_expansion_candidates.tsv)
   • synteny / conserved neighborhoods (link to conserved_neighborhoods.tsv)
   • non-coding RNA census (link to ncRNA_census.tsv) Each row records observation, comparison baseline, literature reference, status (notable / conserved / artifact / negative), and a follow-up test.
6. Produce an interesting-findings section that ranks candidate discoveries relative to the literature-derived baseline and separates:
   • strong candidates with multiple evidence types
   • plausible candidates needing validation
   • likely artifacts or conserved lineage features
   • explicit negative findings where nothing notable was detected
7. Include the comparison baseline, literature context, confidence, and next discriminating analyses for each candidate.

Quick Reference

Input Requirements

Prerequisites:

• Tools declared in the project's pinned Pixi environment. See docs/README.md for expected tools.
• Results tables and metadata are available. Inputs:
• results/.parquet or results/.tsv
• metadata.tsv

Output

• results/bio-stats-ml-reporting/models/
• results/bio-stats-ml-reporting/metrics.tsv
• results/bio-stats-ml-reporting/comparative_axes_summary.tsv
• results/bio-stats-ml-reporting/discovery_summary.tsv
• results/bio-stats-ml-reporting/report.md
• results/bio-stats-ml-reporting/logs/
• results/bio-stats-ml-reporting/prediction_validation.json

Quality Gates

• Model performance sanity checks pass.
• Reference validation passes.
• On execution failure, preserve logs and report the failed command; retry only after diagnosing the cause and recording the changed parameters. Report unmet biological thresholds as results; never tune parameters solely to pass a gate.
• Verify input tables are readable and schema-consistent.
• Discovery summary joins candidate genes/features to annotation evidence, comparison baseline, literature context, and confidence.
• comparative_axes_summary.tsv covers all five mandatory axes (genome-property frontier, marker-gene census, family copy-number, synteny/neighborhoods, ncRNA census) for every query genome, with rows for axes that produced negative findings.
• Final report states what is interesting, what is conserved/expected, what is likely artifact, and what should be tested next.
• Grouped splits have no sample or group overlap, calibration is reported, confounding and imbalance are quantified, and the model is compared with a declared null baseline.