{
  "specification": {
    "reference": "TK1151/GWHBCHF-derived display reference; VCF Chr01-08 preserved in source, numeric derivative chr1-8",
    "source_VCF": "/home/whj/rubber_dandelion_omics/build_runtime/resequencing_variants_CRA009020_20260829/variants/CRA009020_TK1151.pass.vcf.gz",
    "samples_before_QC": 126,
    "trait": "natural rubber content %",
    "source_phenotype": "Yang et al. 2023 additional workbook Table S7 column C",
    "sample_evidence": "128 exact unique counts; 2 parents excluded; R09 unconfirmed excluded",
    "population": "one biparental F1 family; exploratory additive association",
    "QC": {
      "biallelic_SNPs_only": true,
      "chromosomes": [
        1,
        2,
        3,
        4,
        5,
        6,
        7,
        8
      ],
      "minimum_sample_genotype_DP": 5,
      "maximum_variant_missingness": 0.1,
      "minimum_MAF": 0.05,
      "maximum_sample_missingness": 0.15,
      "HWE_filter": "not applied to F1 family",
      "LD_pruning": {
        "window_kb": 50,
        "step_variants": 5,
        "r2": 0.2
      },
      "minimum_observed_genotype_classes": 2,
      "reason": "F1 fixed heterozygosity may have MAF0.5 but no dosage variability; exclude unidentifiable effects before association fitting"
    },
    "models": {
      "GLM": "PLINK1.9 additive linear model; intercept + PC1-PC3",
      "MLM": "GCTA MLMA; additive effect + intercept + PC1-PC3 + genomic relationship random effect"
    },
    "shared_inputs": "same final QC markers/samples; PCA/kinship built once; GRM from LD-pruned set",
    "thresholds": {
      "Bonferroni": "0.05/number of valid tests per model",
      "suggestive": "1/number of valid tests",
      "BH_FDR": "q<=0.05 reported separately"
    },
    "resource_request": {
      "scheduler": "Slurm normal",
      "cpus": 2,
      "memory_GiB": 4,
      "GPU": false
    },
    "source_inputs_read_only": true,
    "scientific_limits": [
      "Read-count supported material identity; author bin genotype consistency unresolved",
      "Single family, limited population extrapolation; association is not causation",
      "Mean phenotype only; raw replicates/environment details unavailable"
    ],
    "planned_validation": [
      "VCF/phenotype exact sample strings, exclusion policy and source hashes",
      "post-QC final sample/marker calls/alleles",
      "sample order identical for PCA, GRM and both models",
      "compare selected independent regressions/model effect/p-value calculations",
      "QQ/calibration, phenotype residuals, valid p-values, true n",
      "plots align with complete downloadable statistics",
      "real public queries/downloads/bilingual rendered desktop/mobile"
    ]
  },
  "actual_run": {
    "samples": 126,
    "QC_SNPs": 1109918,
    "per_chr_QC_counts": {
      "1": 188379,
      "2": 159241,
      "3": 164713,
      "4": 127504,
      "5": 109120,
      "6": 128372,
      "7": 131783,
      "8": 102199
    },
    "final_sample_ids": [
      "F1-1",
      "F1-2",
      "F1-5",
      "F1-6",
      "F1-7",
      "F1-8",
      "F1-9",
      "F1-11",
      "F1-12",
      "F1-13",
      "F1-15",
      "F1-16",
      "F1-18",
      "F1-19",
      "F1-20",
      "F1-21",
      "F1-26",
      "F1-29",
      "F1-30",
      "F1-31",
      "F1-32",
      "F1-33",
      "F1-34",
      "F1-36",
      "F1-37",
      "F1-38",
      "F1-40",
      "F1-41",
      "F1-42",
      "F1-43",
      "F1-44",
      "F1-45",
      "F1-46",
      "F1-48",
      "F1-49",
      "F1-51",
      "F1-53",
      "F1-55",
      "F1-56",
      "F1-58",
      "F1-61",
      "F1-62",
      "F1-63",
      "F1-64",
      "F1-65",
      "F1-66",
      "F1-68",
      "F1-71",
      "F1-72",
      "F1-73",
      "F1-74",
      "F1-75",
      "F1-76",
      "F1-77",
      "F1-78",
      "F1-79",
      "F1-80",
      "F1-81",
      "F1-82",
      "F1-83",
      "F1-84",
      "F1-85",
      "F1-86",
      "F1-87",
      "F1-88",
      "F1-89",
      "F1-90",
      "F1-91",
      "F1-92",
      "F1-93",
      "F1-94",
      "F1-95",
      "F1-96",
      "F1-97",
      "F1-98",
      "F1-99",
      "F1-100",
      "F1-101",
      "F1-102",
      "F1-103",
      "F1-104",
      "F1-105",
      "F1-106",
      "F1-107",
      "F1-108",
      "F1-109",
      "F1-110",
      "F1-111",
      "F1-112",
      "F1-113",
      "F1-114",
      "F1-115",
      "F1-116",
      "F1-117",
      "F1-118",
      "F1-119",
      "F1-120",
      "F1-121",
      "F1-122",
      "F1-123",
      "F1-124",
      "F1-125",
      "F1-126",
      "F1-127",
      "F1-128",
      "F1-129",
      "F1-130",
      "F1-131",
      "F1-132",
      "F1-133",
      "F1-134",
      "F1-135",
      "F1-136",
      "F1-137",
      "F1-138",
      "F1-139",
      "F1-140",
      "F1-141",
      "F1-142",
      "F1-143",
      "F1-144",
      "F1-145",
      "F1-146",
      "F1-147",
      "F1-148",
      "F1-149"
    ],
    "pruned_SNPs": 434572,
    "models": [
      "GLM",
      "MLM"
    ],
    "source_VCF": "/home/whj/rubber_dandelion_omics/build_runtime/resequencing_variants_CRA009020_20260829/variants/CRA009020_TK1151.pass.vcf.gz",
    "source_VCF_bytes": 18246511770,
    "finished_at": "2026-10-14T11:15:50.722643+08:00",
    "variant_QC": "DP>=5; missing<=0.1; MAF>=0.05; biallelic SNP Chr01-08",
    "sample_QC": "missing<=0.15",
    "covariates": [
      "PC1",
      "PC2",
      "PC3"
    ],
    "kinship": "GCTA standardized GRM from LD-pruned markers",
    "identity_policy": "unique exact FASTQ reads correspondence; parents/R09 excluded; author bin input unresolved",
    "actual_scheduler_allocation": {
      "job_id": "154",
      "cpus": "12",
      "memory_MB": "6144",
      "GPU": false,
      "QC_workers": 6
    },
    "dosage_variability_QC": {
      "markers_before": 1111311,
      "nonsegregating_dosage_removed": 1393,
      "markers_after": 1109918,
      "criterion": "at least2 observed diploid genotype classes; constant heterozygosity excluded; no phenotype based selection"
    },
    "original_source_full_checksum": {
      "source_path": "/home/whj/rubber_dandelion_omics/build_runtime/resequencing_variants_CRA009020_20260829/variants/CRA009020_TK1151.pass.vcf.gz",
      "source_bytes": 18246511770,
      "source_sha256": "68da4ddabaff5358462c23f69f71eb6980c4faff0c2666415e0e8b6d89a719bc",
      "source_stat_unchanged": true,
      "aligned_native_first_block_equal": true,
      "elapsed_seconds": 3611.4901111125946
    }
  },
  "software": {
    "plink19": "PLINK v1.90b7.2 64-bit (11 Dec 2023)\n",
    "gcta": "*******************************************************************\n* Genome-wide Complex Trait Analysis (GCTA)\n* version v1.95.1 Linux\n* Built at Feb  2 2026 16:51:42, by GCC 8.4\n* (C) 2010-present, Yang Lab, Westlake University\n* Please report bugs to Jian Yang <jian.yang@westlake.edu.cn>\n*******************************************************************\nAnalysis started at 09:07:41 CST on Wed Oct 14 2026.\nHostname: SuperServer\n\nWarning: Warning: No output file specified. Using default output file 'output'.\nAccepted options:\nError: \n  invalid option \"--version\".\n\nAn error occurs, please che",
    "bcftools": "bcftools 1.13\nUsing htslib 1.13+ds\nCopyright (C) 2021 Genome Research Ltd.\nLicense Expat: The MIT/Expat license\nThis is free software: you are free to change and redistribute it.\nThere is NO WARRANTY, to the extent permitted by law.\n"
  },
  "raw_result_columns": {
    "GLM": [
      "CHR",
      "SNP",
      "BP",
      "A1",
      "TEST",
      "NMISS",
      "BETA",
      "SE",
      "L95",
      "U95",
      "STAT",
      "P"
    ],
    "MLM": [
      "Chr",
      "SNP",
      "bp",
      "A1",
      "A2",
      "Freq",
      "b",
      "se",
      "p"
    ]
  },
  "gene_annotation": {
    "source": "/home/whj/rubber_dandelion_omics/build_runtime/resequencing_variants_CRA009020_20260829/variants/CRA009020_gene_variants.sqlite3",
    "reference": "TK1151",
    "gene_records": 45224,
    "nearest_gene_definition": "overlapping gene interval, else minimum distance to stored interval boundary; proximity only",
    "source_coordinate_export": "reference_gene_coordinates.tsv inside workflow.zip",
    "coordinate_export_SHA256": "dc45eb73fa30746f11ef9ccd4aefafa637c8c3f8f853bcc593f1e5e3b4489121"
  },
  "site_interpretation": "single-family exploratory association; author bin genotype consistency remains unresolved",
  "threshold_display_revision": {
    "default": "screening",
    "p_threshold": 0.0001,
    "minus_log10_p": 4.0,
    "basis": "user-specified fixed exploratory screening threshold",
    "empirical_calibration_performed": false,
    "original_association_values_unchanged": true,
    "retained_references": [
      "suggestive 1/M",
      "Bonferroni 0.05/M",
      "BH FDR q<=0.05"
    ]
  },
  "candidate_gene_policy": {
    "p_threshold": 0.0001,
    "gene_assignment": "reuse existing nearest / overlapping gene mapping, exact native IDs and gene coordinates",
    "unique_union_genes": 206,
    "genes_supported_by_both_models": 131,
    "not_causal_validation": true,
    "no_LD_window_invented": true,
    "source_annotation_verified": true
  }
}