Changelog
0.5.1
- Added native pedigree JSON template to support direct construction of pedigree files in
clinical-genetics.
0.5.0
Added clinical-genetics guidance for structured pedigree data and family-based interpretation.
- Added the
clinical-geneticsAgent Skill. - Added guidance for pedigree identity, typed family and reproductive relationships, clinical states, segregation, and genomic findings.
- Added interoperability guidance for FHIR, EHR, biobank, and PLINK workflows.
- Updated routing and documentation for the new domain.
0.4.0
Expanded Biology Skills with expert guidance for measurement validity, experimental design, structural biology, and biological statistics.
- Added
experimental-design,structural-biology, andbiological-statisticsAgent Skills. - Added guidance for observability and negative evidence, identifier mapping and join cardinality, genomic callability, and population-frequency interpretation.
- Added structural guidance for residue identity, isoforms, experimental constructs, predicted structures, and confidence metrics.
- Added statistical guidance for experimental units, pseudoreplication, ascertainment, selection, denominators, and target populations.
- Updated skill routing and documentation for the expanded domain set.
0.3.0
Added synthetic-biology guidance for personalised mRNA vaccine design.
- Added the
synthetic-biologyAgent Skill. - Added guidance for neoantigen identity, peptide:HLA interpretation, target-set selection under uncertainty, and mRNA polyepitope construct design.
- Added clearer separation between biological observations, predictions, selected targets, engineered constructs, and downstream outcomes.
- Updated routing and documentation for the new domain.
0.2.0
Expanded Biology Skills with bioinformatics and causal-inference guidance.
- Added
bioinformaticsandquinary-inferenceAgent Skills. - Added guidance for metadata, provenance, sample identity, QC outputs, qualifying evidence, and qualifying variants.
- Expanded genomics coverage for sequencing files, intervals, alignments, variant calls, HGVS nomenclature, coding consequences, and reference provenance.
- Added support for QEM and QVSS concepts.
- Updated routing and repository documentation.
0.1.0
Initial public release.
- Added
biology-coreandgenomicsAgent Skills. - Added foundational references for biological context, evidence, identifiers, reference genomes, variants, transcripts, inheritance, phase, and gene expression.
- Added contribution, governance, validation, testing, and release infrastructure.