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Start with the package README for installation and examples. These documents describe the supported workflow; qualification reports retain the versions, fixtures, and limits of their original measurements.

Authoritative contracts

The installed R help is authoritative for public arguments and return values: reference, VCF import, founders, pedigree simulation, phenotypes, gene sets, printing, pedigree domains, and record workloads.

Pedigree record generators supply deterministic solver workloads. Their latent parent-average values are not exact draws from a pedigree relationship covariance. Genotype-based phenotype simulation is a separate workflow.

Examples and development

  • Composable breeding workflow uses a tiny synthetic phased panel, native selection/meiosis, genomic records, parent retention and matched or mismatched pools. No external predictor is fitted; an external caller can supply its predictions for selection.

  • 1000 Genomes chromosome 22 is a complete GRCh37 example that downloads official reference/map inputs when absent.

  • End-to-end phenotypes constructs a small synthetic local fixture. Run after library(gsim) with qgg installed; its illustrative LD scores are not estimates from real 1000G data.

  • Controlled gene sets uses existing simulated causal SNP truth and an explicitly synthetic SNP?gene mapping; no downloads.

  • Repository instructions describe installation, explicitly loading an isolated installed package for focused tests, and generated Rd.

  • Copyrights and provenance retain HAPNEST attribution and applicable gbits/gmat notices.

qgg is optional generally and used to construct Glist objects. Supported BED Glist accumulation is standalone and bounded; see the phenotype contract for selection, storage, memory and custom-reader limits. HAP phenotype input and gsuite-generated Glist compatibility are not established.

Qualification and reproducibility

Reports retain the scope and revision of their own qualification. Historical recommendations are scoped to their measured revisions.

Evidence Scope and reproduction
Bounded Glist accumulation 0.15.0 focused parity, malformed-input and bounded resource checks; script.
Genotypes to phenotypes Small local fixture, qgg dosage/ID parity and phenotype controls; example and test.
Founder chromosome identity Exact byte/audit comparisons and intentional replacement of block-index streams; tests.
Pedigree meiosis Byte oracle, Mendelian consistency, and uncertainty-based relationship experiment; tests.
Deferred HAPNEST comparison Pinned external oracle, prerequisites, proposed fixture and acceptance rules; comparison has not passed or run.
Production chromosome 22 benchmark Real 1000G inputs, checksums, measured revision/environment and timing uncertainty; script.
Batched/parallel founder benchmark Real 1000G prepared panel, plus a separately labelled synthetic 0.12 guard; script.
Parallel scaling diagnosis Synthetic 49,000-marker panel, not 1000G LD; counter limitations and removed external fixture are explicit; same benchmark script.

The 50,000-animal record-workload script reports construction sizes, times, and checksums, not covariance recovery or solver performance. Current tests, both examples, and all benchmark/qualification scripts remain available. Benchmarks and broad qualification require authorization; nothing in this index claims they were rerun during documentation cleanup.

Authoritative source