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Changelog

1.0.0 — 2026-09-28

First release: the v1.0 goals of the master plan (§1.1), built and validated phase by phase (P0–P8).

Formats (P1–P2). Readers for IDAT (plain or gzipped; encrypted v1 refused), BPM, CSV manifest, EGT, GTC v3–v5 and sample sheets; simurg inspect; raw X/Y assembly into a canonical Parquet model (simurg ingest, resumable).

Signal and calling (P3–P4). Per-bin affine normalization 1.2.0 and 1.1.2; GenCall-equivalent calling from an EGT with GenCall score; θ/R, BAF, LRR, LogR deviation, GC10/GC50, intensity percentiles, sex (rules 1 and 2); GTC v5/v3 writer (simurg genotype). Presets current and autocall-1.6.2.

QC (P5). Control-probe metrics, threshold profiles and YAML, two-axis sample status and flags, BAF-regression contamination, KING-robust relatedness and Mendel errors, locus summary, threshold suggestion, a self-contained HTML QC report with xlsx/csv table (simurg qc …).

Outputs (P6). Plus-strand harmonisation with an audit trail; per-sample VCF.gz + tabix or cohort BCF + CSI (GT:GS:BAF:LRR, optional INFO and intensity fields, merged multi-probe sites, indels from SourceSeq, SNV+indel merging, auxiliary MNV loci); PLINK 1 .bed and PLINK 2 .pgen; BAF/LRR bedGraph; final report and genotype matrix.

Testing (P7). simurg compare (EXACT/NEAR/DISCREPANCY/UNKNOWN per field and locus class, HTML dashboard) and a nightly differential run against gtc2vcf, GTCtoVCF and vendor GTCs.

Validation (P8). 360 GSA arrays of 120 1000 Genomes individuals vs NYGC 30x WGS (concordance 0.9934) and GIAB HG001 (0.9985, non-ref F1 0.997); replicate concordance 0.9966. Vendor-equivalence: 2138/2141 Omni2.5 GTCs byte-identical, zero unexplained VCF/PLINK differences vs gtc2vcf, GTCtoVCF and plink2.

Documentation: docs/user_guide.md, examples/, docs/validation/P1.md … P8.md, docs/known_unknowns.md, docs/messages.md.

Known limitations: needs an existing cluster file (training is v2); no CN/LOH/PGx yet; largest tested cohort 2141 samples; pure NumPy speed.