{
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  "Package": "GeneTrackR",
  "Type": "Package",
  "Title": "Genomic Track Visualization and Haplotype Analysis",
  "Version": "0.99.2",
  "Date": "2026-09-01",
  "Authors@R": "person(given = \"Shuchao\", family = \"Ren\", role = c(\"aut\", \"cre\"),\nemail = \"rensc0718@163.com\")",
  "Description": "Provides tools to read, validate, query, transform, write,\nand visualize gene annotations, genomic signal tracks, and\nvariant tracks using a shared genomic coordinate framework.\nSupports GenePred, GTF, GFF3, and BED annotations; bedGraph,\nwig, and bigWig signals; VCF variants; integrated locus\nvisualization; haplotype construction; phenotype association;\nlinkage disequilibrium; haplotype refinement; and\nvariant-effect analysis. The package interoperates with\nGenomicRanges objects and uses a pure-R signal I/O layer so\ncore workflows do not require a compiled extension.",
  "License": "GPL-3",
  "URL": "https://renscq.github.io/GeneTrackR/,\nhttps://github.com/Renscq/GeneTrackR",
  "BugReports": "https://github.com/Renscq/GeneTrackR/issues",
  "biocViews": "Software, GenomeAnnotation, VariantAnnotation, Coverage,\nSequencing, Visualization",
  "Encoding": "UTF-8",
  "Roxygen": "list(markdown = TRUE)",
  "VignetteBuilder": "knitr",
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  "NeedsCompilation": "no",
  "Config/roxygen2/version": "8.1.0",
  "Repository": "https://biocstaging.r-universe.dev",
  "Date/Publication": "2026-09-01 09:05:02 UTC",
  "RemoteUrl": "https://github.com/BiocStaging/GeneTrackR",
  "RemoteRef": "HEAD",
  "RemoteSha": "5d4a1b2b9dc145527eafe4a201bc5d838feeffb5",
  "Packaged": {
    "Date": "2026-10-01 12:58:19 UTC",
    "User": "root"
  },
  "Author": "Shuchao Ren [aut, cre]",
  "Maintainer": "Shuchao Ren <rensc0718@163.com>",
  "_user": "biocstaging",
  "_type": "src",
  "_file": "GeneTrackR_0.99.2.tar.gz",
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  "_expires": "2027-01-09T13:24:15.000Z",
  "_created": "2026-10-01T12:58:19.000Z",
  "_published": "2026-10-01T13:24:18.140Z",
  "_bioccheck": {
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    "warning": 0,
    "note": 5
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  "_host": "GitHub-Actions",
  "_buildurl": "https://github.com/r-universe/biocstaging/actions/runs/36864789770",
  "_status": "success",
  "_upstream": "https://github.com/BiocStaging/GeneTrackR",
  "_commit": {
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    "author": "rensc <rensc0718@163.com>",
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    "message": "0.99.2\nGeneTrackR-0.99.2-submission-clean-source\n",
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  "_maintainer": {
    "name": "Shuchao Ren",
    "email": "rensc0718@163.com",
    "login": "renscq",
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    "uuid": 35422764
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  "_updates": [
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  "_tags": [],
  "_topics": [
    "software",
    "genomeannotation",
    "variantannotation",
    "coverage",
    "sequencing",
    "visualization"
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  "_stars": 0,
  "_contributors": [
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    "source": "https://cranlogs.r-pkg.org/downloads/total/last-month/GeneTrackR"
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  "_devurl": "https://github.com/renscq/genetrackr",
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  "_assets": [
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  "_exports": [
    "as_exon_table",
    "as_feature",
    "as_feature_table",
    "as_gene_table",
    "as_genepred",
    "as_granges",
    "as_transcript_table",
    "benchmark_tabix_query",
    "bin_bwg",
    "BwgTrack",
    "compute_ld_block",
    "diagnose_tabix",
    "Feature",
    "FeatureTrack",
    "GenePred",
    "get_gene_length_distribution_table",
    "get_genepred_length_table",
    "hap_gene_variant",
    "hap_region_variant",
    "hap_variant",
    "LDTrack",
    "merge_bwg",
    "merge_feature",
    "norm_bwg",
    "plot_feature_track",
    "plot_gene",
    "plot_gene_length_distribution",
    "plot_genepred_length_distribution",
    "plot_hap_pheno",
    "plot_hap_refined",
    "plot_hap_variant",
    "plot_ld_block",
    "plot_pheno",
    "plot_refined_hap_pheno",
    "plot_refined_hap_variant",
    "plot_region",
    "plot_signal_gene",
    "plot_signal_region",
    "plot_signal_transcript",
    "plot_tracks",
    "plot_transcript",
    "plot_variant",
    "plot_variant_effect",
    "plot_variant_pheno",
    "plot_variant_track",
    "read_bed",
    "read_bwg",
    "read_genepred",
    "read_gff",
    "read_gtf",
    "read_pheno",
    "read_vcf",
    "read_vcf_track",
    "refine_haplotype",
    "retrieve_bwg",
    "retrieve_feature",
    "retrieve_vcf",
    "seqinfo_bwg",
    "slice_bwg",
    "summary_bwg",
    "summary_feature",
    "summary_pheno",
    "summary_vcf",
    "validate_bwg",
    "validate_feature",
    "validate_vcf",
    "VariantTrack",
    "write_bwg",
    "write_feature",
    "write_feature_track",
    "write_genepred",
    "write_variant_track",
    "write_vcf"
  ],
  "_help": [
    {
      "page": "as_exon_table",
      "title": "Extract exon table from a GenePred object",
      "topics": [
        "as_exon_table"
      ]
    },
    {
      "page": "as_feature",
      "title": "Coerce an annotation object to a unified Feature object",
      "topics": [
        "as_feature",
        "as_feature.data.frame",
        "as_feature.Feature",
        "as_feature.FeatureTrack",
        "as_feature.GenePred"
      ]
    },
    {
      "page": "as_feature_table",
      "title": "Extract the standardized feature table",
      "topics": [
        "as_feature_table"
      ]
    },
    {
      "page": "as_gene_table",
      "title": "Extract gene table from a GenePred object",
      "topics": [
        "as_gene_table"
      ]
    },
    {
      "page": "as_genepred",
      "title": "Convert a Feature object with gene-model information to GenePred",
      "topics": [
        "as_genepred"
      ]
    },
    {
      "page": "as_granges",
      "title": "Convert a GeneTrackR genomic track object to GRanges",
      "topics": [
        "as_granges"
      ]
    },
    {
      "page": "as_transcript_table",
      "title": "Extract transcript table from a GenePred object",
      "topics": [
        "as_transcript_table"
      ]
    },
    {
      "page": "benchmark_tabix_query",
      "title": "Test whether a bedGraph tabix query returns records without full-file fallback",
      "topics": [
        "benchmark_tabix_query"
      ]
    },
    {
      "page": "bin_bwg",
      "title": "Bin signal tracks into fixed-width windows",
      "topics": [
        "bin_bwg"
      ]
    },
    {
      "page": "BwgTrack",
      "title": "Create a BwgTrack object",
      "topics": [
        "BwgTrack"
      ]
    },
    {
      "page": "compute_ld_block",
      "title": "Compute a linkage disequilibrium block from VCF genotypes",
      "topics": [
        "compute_ld_block"
      ]
    },
    {
      "page": "diagnose_tabix",
      "title": "Diagnose tabix availability for bedGraph tracks",
      "topics": [
        "diagnose_tabix"
      ]
    },
    {
      "page": "Feature",
      "title": "Create a standardized Feature object",
      "topics": [
        "Feature"
      ]
    },
    {
      "page": "FeatureTrack",
      "title": "Create a FeatureTrack object",
      "topics": [
        "FeatureTrack"
      ]
    },
    {
      "page": "GenePred",
      "title": "Create a GenePred object",
      "topics": [
        "GenePred"
      ]
    },
    {
      "page": "GeneTrackR-advanced-parameters",
      "title": "Advanced parameter guide for GeneTrackR",
      "topics": [
        "GeneTrackR-advanced-parameters"
      ]
    },
    {
      "page": "GeneTrackR-demo-data",
      "title": "GeneTrackR deterministic demo files",
      "topics": [
        "GeneTrackR-demo-data"
      ]
    },
    {
      "page": "get_gene_length_distribution_table",
      "title": "Extract length records from a gene annotation object",
      "topics": [
        "get_genepred_length_table",
        "get_gene_length_distribution_table"
      ]
    },
    {
      "page": "hap_gene_variant",
      "title": "Build haplotypes from variants in a gene or transcript region",
      "topics": [
        "hap_gene_variant"
      ]
    },
    {
      "page": "hap_region_variant",
      "title": "Build haplotypes from variants in a genomic region",
      "topics": [
        "hap_region_variant"
      ]
    },
    {
      "page": "hap_variant",
      "title": "Build haplotypes from variants in a gene, transcript, or genomic region",
      "topics": [
        "hap_variant"
      ]
    },
    {
      "page": "head.BwgTrack",
      "title": "Show the first rows of a BwgTrack object",
      "topics": [
        "head.BwgTrack"
      ]
    },
    {
      "page": "LDTrack",
      "title": "Create an LDTrack object",
      "topics": [
        "LDTrack"
      ]
    },
    {
      "page": "merge_bwg",
      "title": "Merge signal track objects",
      "topics": [
        "merge_bwg"
      ]
    },
    {
      "page": "merge_feature",
      "title": "Merge annotation feature objects",
      "topics": [
        "merge_feature"
      ]
    },
    {
      "page": "norm_bwg",
      "title": "Normalize signal tracks",
      "topics": [
        "norm_bwg"
      ]
    },
    {
      "page": "plot_feature_track",
      "title": "Plot a FeatureTrack object",
      "topics": [
        "plot_feature_track"
      ]
    },
    {
      "page": "plot_gene",
      "title": "Plot a gene structure",
      "topics": [
        "plot_gene"
      ]
    },
    {
      "page": "plot_gene_length_distribution",
      "title": "Plot gene annotation feature length distributions",
      "topics": [
        "plot_genepred_length_distribution",
        "plot_gene_length_distribution"
      ]
    },
    {
      "page": "plot_hap_pheno",
      "title": "Plot phenotype values grouped by haplotype",
      "topics": [
        "plot_hap_pheno"
      ]
    },
    {
      "page": "plot_hap_refined",
      "title": "Plot phenotype distributions for refined haplotypes",
      "topics": [
        "plot_hap_refined"
      ]
    },
    {
      "page": "plot_hap_variant",
      "title": "Plot gene variants and haplotype table",
      "topics": [
        "plot_hap_variant"
      ]
    },
    {
      "page": "plot_ld_block",
      "title": "Plot a triangular LD heatmap",
      "topics": [
        "plot_ld_block"
      ]
    },
    {
      "page": "plot_pheno",
      "title": "Plot phenotype distributions",
      "topics": [
        "plot_pheno"
      ]
    },
    {
      "page": "plot_refined_hap_pheno",
      "title": "Plot phenotype distributions for refined haplotypes",
      "topics": [
        "plot_refined_hap_pheno"
      ]
    },
    {
      "page": "plot_refined_hap_variant",
      "title": "Plot grouped variant table for refined haplotypes",
      "topics": [
        "plot_refined_hap_variant"
      ]
    },
    {
      "page": "plot_region",
      "title": "Plot gene structures in a genomic region",
      "topics": [
        "plot_region"
      ]
    },
    {
      "page": "plot_signal_gene",
      "title": "Plot signal over a gene",
      "topics": [
        "plot_signal_gene"
      ]
    },
    {
      "page": "plot_signal_region",
      "title": "Plot signal over a genomic region",
      "topics": [
        "plot_signal_region"
      ]
    },
    {
      "page": "plot_signal_transcript",
      "title": "Plot signal over a transcript",
      "topics": [
        "plot_signal_transcript"
      ]
    },
    {
      "page": "plot_tracks",
      "title": "Plot combined signal and gene model tracks",
      "topics": [
        "plot_tracks"
      ]
    },
    {
      "page": "plot_transcript",
      "title": "Plot a transcript structure",
      "topics": [
        "plot_transcript"
      ]
    },
    {
      "page": "plot_variant",
      "title": "Plot variants in a genomic region",
      "topics": [
        "plot_variant"
      ]
    },
    {
      "page": "plot_variant_effect",
      "title": "Plot phenotype effect size of each natural variant",
      "topics": [
        "plot_variant_effect"
      ]
    },
    {
      "page": "plot_variant_pheno",
      "title": "Plot phenotype values grouped by a single variant genotype",
      "topics": [
        "plot_variant_pheno"
      ]
    },
    {
      "page": "plot_variant_track",
      "title": "Plot a VariantTrack object",
      "topics": [
        "plot_variant_track"
      ]
    },
    {
      "page": "print.GeneTrackRPhenoPlot",
      "title": "Print GeneTrackR phenotype plot result",
      "topics": [
        "print.GeneTrackRPhenoPlot"
      ]
    },
    {
      "page": "read_bed",
      "title": "Read a BED file as a FeatureTrack",
      "topics": [
        "read_bed"
      ]
    },
    {
      "page": "read_bwg",
      "title": "Read bedGraph, wig, or bigWig signal tracks",
      "topics": [
        "read_bwg"
      ]
    },
    {
      "page": "read_genepred",
      "title": "Read a GenePred annotation file",
      "topics": [
        "read_genepred"
      ]
    },
    {
      "page": "read_gff",
      "title": "Read a GFF3 file as a FeatureTrack",
      "topics": [
        "read_gff"
      ]
    },
    {
      "page": "read_gtf",
      "title": "Read a GTF file as a FeatureTrack",
      "topics": [
        "read_gtf"
      ]
    },
    {
      "page": "read_pheno",
      "title": "Read a phenotype table",
      "topics": [
        "read_pheno"
      ]
    },
    {
      "page": "read_vcf",
      "title": "Read a VCF file as a VariantTrack",
      "topics": [
        "read_vcf"
      ]
    },
    {
      "page": "read_vcf_track",
      "title": "Read a VCF file as a VariantTrack",
      "topics": [
        "read_vcf_track"
      ]
    },
    {
      "page": "refine_haplotype",
      "title": "Refine haplotypes by phenotype similarity",
      "topics": [
        "refine_haplotype"
      ]
    },
    {
      "page": "retrieve_bwg",
      "title": "Retrieve signal records from a BwgTrack object",
      "topics": [
        "retrieve_bwg"
      ]
    },
    {
      "page": "retrieve_feature",
      "title": "Retrieve annotation features or sub-objects",
      "topics": [
        "retrieve_feature"
      ]
    },
    {
      "page": "retrieve_vcf",
      "title": "Retrieve variants from a VariantTrack or an indexed VCF file",
      "topics": [
        "retrieve_vcf"
      ]
    },
    {
      "page": "seqinfo_bwg",
      "title": "Get chromosome information from BwgTrack objects",
      "topics": [
        "seqinfo_bwg"
      ]
    },
    {
      "page": "slice_bwg",
      "title": "Slice signal tracks by genomic region",
      "topics": [
        "slice_bwg"
      ]
    },
    {
      "page": "summary_bwg",
      "title": "Summarize signal tracks within a region",
      "topics": [
        "summary_bwg"
      ]
    },
    {
      "page": "summary_feature",
      "title": "Summarize a Feature-compatible annotation object",
      "topics": [
        "summary_feature"
      ]
    },
    {
      "page": "summary_pheno",
      "title": "Summarize phenotype traits",
      "topics": [
        "summary_pheno"
      ]
    },
    {
      "page": "summary_vcf",
      "title": "Summarize a VariantTrack object",
      "topics": [
        "summary_vcf"
      ]
    },
    {
      "page": "validate_bwg",
      "title": "Validate a BwgTrack object",
      "topics": [
        "validate_bwg"
      ]
    },
    {
      "page": "validate_feature",
      "title": "Validate a Feature annotation object",
      "topics": [
        "validate_feature"
      ]
    },
    {
      "page": "validate_vcf",
      "title": "Validate a VariantTrack object",
      "topics": [
        "validate_vcf"
      ]
    },
    {
      "page": "VariantTrack",
      "title": "Create a VariantTrack object",
      "topics": [
        "VariantTrack"
      ]
    },
    {
      "page": "write_bwg",
      "title": "Write BwgTrack signal data",
      "topics": [
        "write_bwg"
      ]
    },
    {
      "page": "write_feature",
      "title": "Write Feature annotation data",
      "topics": [
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        "Step 4. Inspect the HapRefined object",
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        "Step 6. Plot the refined haplotype structure",
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        "Step 8. Evaluate trait choice and refinement thresholds",
        "A strongly haplotype-associated trait may preserve all groups",
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        "Step 2. Validate and summarize the core objects",
        "Step 3. Inspect the locus in a browser-like view",
        "Step 4. Retrieve the gene-body variants",
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        "Step 2. Export genomic track files",
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        "Step 5. Export the LD matrix cleanly",
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