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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-genetics Agent 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, and biological-statistics Agent 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-biology Agent 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 bioinformatics and quinary-inference Agent 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-core and genomics Agent 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.