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  "Date": "2026-03-18",
  "Title": "Tools for Analyzing QTL Experiments",
  "Author": "Karl W Broman [aut, cre]\n(<https://orcid.org/0000-0002-4914-6671>), Hao Wu [aut], Gary\nChurchill [ctb] (<https://orcid.org/0000-0001-9190-9284>),\nSaunak Sen [ctb] (<https://orcid.org/0000-0003-4519-6361>),\nDanny Arends [ctb] (<https://orcid.org/0000-0001-8738-0162>),\nRobert Corty [ctb], Timothee Flutre [ctb], Ritsert Jansen\n[ctb], Pjotr Prins [ctb]\n(<https://orcid.org/0000-0002-8021-9162>), Lars Ronnegard\n[ctb], Rohan Shah [ctb], Laura Shannon [ctb], Quoc Tran [ctb],\nAaron Wolen [ctb], Brian Yandell [ctb]\n(<https://orcid.org/0000-0002-8774-9377>), R Core Team [ctb]",
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  "Description": "Analysis of experimental crosses to identify genes (called\nquantitative trait loci, QTLs) contributing to variation in\nquantitative traits. Broman et al. (2003)\n<doi:10.1093/bioinformatics/btg112>.",
  "Copyright": "Code for Brent's method for finding the root of a univariate\nfunction was taken from R 2.15.1 (Copyright 1999, 2001 The R\nCore Team)",
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    "simulatemissingdata",
    "stepwiseqtl",
    "strip.partials",
    "subrousummaryscantwo",
    "summary.map",
    "summaryMap",
    "summaryScantwoOld",
    "switch.order",
    "switchAlleles",
    "table2map",
    "top.errorlod",
    "totmar",
    "transformPheno",
    "tryallpositions",
    "typingGap",
    "write.cross",
    "xaxisloc.scanone"
  ],
  "_datasets": [
    {
      "name": "badorder",
      "title": "An intercross with misplaced markers",
      "object": "badorder",
      "file": "badorder.RData",
      "class": [
        "f2",
        "cross"
      ],
      "fields": [],
      "table": false,
      "tojson": false
    },
    {
      "name": "bristle3",
      "title": "Data on bristle number in Drosophila",
      "object": "bristle3",
      "file": "bristle3.RData",
      "class": [
        "bc",
        "cross"
      ],
      "fields": [],
      "table": false,
      "tojson": false
    },
    {
      "name": "bristleX",
      "title": "Data on bristle number in Drosophila",
      "object": "bristleX",
      "file": "bristleX.RData",
      "class": [
        "bc",
        "cross"
      ],
      "fields": [],
      "table": false,
      "tojson": false
    },
    {
      "name": "fake.4way",
      "title": "Simulated data for a 4-way cross",
      "object": "fake.4way",
      "file": "fake.4way.RData",
      "class": [
        "4way",
        "cross"
      ],
      "fields": [],
      "table": false,
      "tojson": false
    },
    {
      "name": "fake.bc",
      "title": "Simulated data for a backcross",
      "object": "fake.bc",
      "file": "fake.bc.RData",
      "class": [
        "bc",
        "cross"
      ],
      "fields": [],
      "table": false,
      "tojson": false
    },
    {
      "name": "fake.f2",
      "title": "Simulated data for an F2 intercross",
      "object": "fake.f2",
      "file": "fake.f2.RData",
      "class": [
        "f2",
        "cross"
      ],
      "fields": [],
      "table": false,
      "tojson": false
    },
    {
      "name": "hyper",
      "title": "Data on hypertension",
      "object": "hyper",
      "file": "hyper.RData",
      "class": [
        "bc",
        "cross"
      ],
      "fields": [],
      "table": false,
      "tojson": false
    },
    {
      "name": "listeria",
      "title": "Data on Listeria monocytogenes susceptibility",
      "object": "listeria",
      "file": "listeria.RData",
      "class": [
        "f2",
        "cross"
      ],
      "fields": [],
      "table": false,
      "tojson": false
    },
    {
      "name": "locations",
      "title": "Genetic locations of traits for the multitrait dataset",
      "object": "locations",
      "file": "locations.RData",
      "class": [
        "data.frame"
      ],
      "fields": [
        "Name",
        "Chr",
        "cM"
      ],
      "rows": 24,
      "table": true,
      "tojson": true
    },
    {
      "name": "map10",
      "title": "An example genetic map",
      "object": "map10",
      "file": "map10.RData",
      "class": [
        "map"
      ],
      "fields": [],
      "table": false,
      "tojson": false
    },
    {
      "name": "mapthis",
      "title": "Simulated data for illustrating genetic map construction",
      "object": "mapthis",
      "file": "mapthis.RData",
      "class": [
        "f2",
        "cross"
      ],
      "fields": [],
      "table": false,
      "tojson": false
    },
    {
      "name": "multitrait",
      "title": "Example Cross object from R/QTL with multiple traits",
      "object": "multitrait",
      "file": "multitrait.RData",
      "class": [
        "riself",
        "cross"
      ],
      "fields": [],
      "table": false,
      "tojson": false
    }
  ],
  "_help": [
    {
      "page": "a.starting.point",
      "title": "Introductory comments on R/qtl",
      "topics": [
        "qtl-package"
      ]
    },
    {
      "page": "add.cim.covar",
      "title": "Indicate marker covariates from composite interval mapping",
      "topics": [
        "add.cim.covar"
      ]
    },
    {
      "page": "add.threshold",
      "title": "Add significance threshold to plot",
      "topics": [
        "add.threshold"
      ]
    },
    {
      "page": "addcovarint",
      "title": "Add QTL x covariate interaction to a multiple-QTL model",
      "topics": [
        "addcovarint"
      ]
    },
    {
      "page": "addint",
      "title": "Add pairwise interaction to a multiple-QTL model",
      "topics": [
        "addint"
      ]
    },
    {
      "page": "addloctocross",
      "title": "Add phenotype location into a cross object",
      "topics": [
        "addloctocross"
      ]
    },
    {
      "page": "addmarker",
      "title": "Add a marker to a cross",
      "topics": [
        "addmarker"
      ]
    },
    {
      "page": "addpair",
      "title": "Scan for an additional pair of QTL in a multiple-QTL model",
      "topics": [
        "addpair"
      ]
    },
    {
      "page": "addqtl",
      "title": "Scan for an additional QTL in a multiple-QTL model",
      "topics": [
        "addqtl"
      ]
    },
    {
      "page": "addtoqtl",
      "title": "Add to a qtl object",
      "topics": [
        "addtoqtl"
      ]
    },
    {
      "page": "allchrsplits",
      "title": "Test all possible splits of a chromosome into two pieces",
      "topics": [
        "allchrsplits"
      ]
    },
    {
      "page": "argmax.geno",
      "title": "Reconstruct underlying genotypes",
      "topics": [
        "argmax.geno"
      ]
    },
    {
      "page": "arithscan",
      "title": "Arithmetic operators for scanone and scantwo results",
      "topics": [
        "+.scanone",
        "+.scantwo",
        "-.scanone",
        "-.scantwo"
      ]
    },
    {
      "page": "arithscanperm",
      "title": "Arithmetic Operators for permutation results",
      "topics": [
        "+.scanoneperm",
        "+.scantwoperm",
        "-.scanoneperm",
        "-.scantwoperm"
      ]
    },
    {
      "page": "badorder",
      "title": "An intercross with misplaced markers",
      "topics": [
        "badorder"
      ]
    },
    {
      "page": "bayesint",
      "title": "Bayesian credible interval",
      "topics": [
        "bayesint"
      ]
    },
    {
      "page": "bristle3",
      "title": "Data on bristle number in Drosophila",
      "topics": [
        "bristle3"
      ]
    },
    {
      "page": "bristleX",
      "title": "Data on bristle number in Drosophila",
      "topics": [
        "bristleX"
      ]
    },
    {
      "page": "c.cross",
      "title": "Combine data for QTL experiments",
      "topics": [
        "c.cross"
      ]
    },
    {
      "page": "c.scanone",
      "title": "Combine columns from multiple scanone results",
      "topics": [
        "c.scanone",
        "cbind.scanone"
      ]
    },
    {
      "page": "c.scanoneperm",
      "title": "Combine data from scanone permutations",
      "topics": [
        "c.scanoneperm",
        "rbind.scanoneperm"
      ]
    },
    {
      "page": "c.scantwo",
      "title": "Combine columns from multiple scantwo results",
      "topics": [
        "c.scantwo",
        "cbind.scantwo"
      ]
    },
    {
      "page": "c.scantwoperm",
      "title": "Combine data from scantwo permutations",
      "topics": [
        "c.scantwoperm",
        "rbind.scantwoperm"
      ]
    },
    {
      "page": "calc.errorlod",
      "title": "Identify likely genotyping errors",
      "topics": [
        "calc.errorlod"
      ]
    },
    {
      "page": "calc.genoprob",
      "title": "Calculate conditional genotype probabilities",
      "topics": [
        "calc.genoprob"
      ]
    },
    {
      "page": "calc.penalties",
      "title": "Calculate LOD penalties",
      "topics": [
        "calc.penalties"
      ]
    },
    {
      "page": "cbind.scanoneperm",
      "title": "Combine columns from multiple scanone permutation results",
      "topics": [
        "cbind.scanoneperm"
      ]
    },
    {
      "page": "cbind.scantwoperm",
      "title": "Combine scantwo permutations by column",
      "topics": [
        "cbind.scantwoperm"
      ]
    },
    {
      "page": "checkAlleles",
      "title": "Identify markers with switched alleles",
      "topics": [
        "checkAlleles"
      ]
    },
    {
      "page": "chrlen",
      "title": "Chromosome lengths in QTL experiment",
      "topics": [
        "chrlen"
      ]
    },
    {
      "page": "chrnames",
      "title": "Pull out the chromosome names from a cross",
      "topics": [
        "chrnames"
      ]
    },
    {
      "page": "cim",
      "title": "Composite interval mapping",
      "topics": [
        "cim"
      ]
    },
    {
      "page": "clean.cross",
      "title": "Remove derived data",
      "topics": [
        "clean.cross"
      ]
    },
    {
      "page": "clean.scantwo",
      "title": "Clean up scantwo output",
      "topics": [
        "clean.scantwo"
      ]
    },
    {
      "page": "cleanGeno",
      "title": "Delete genotypes that are possibly in error",
      "topics": [
        "cleanGeno"
      ]
    },
    {
      "page": "comparecrosses",
      "title": "Compare two cross objects",
      "topics": [
        "comparecrosses"
      ]
    },
    {
      "page": "comparegeno",
      "title": "Compare individuals' genotype data",
      "topics": [
        "comparegeno"
      ]
    },
    {
      "page": "compareorder",
      "title": "Compare two orderings of markers on a chromosome",
      "topics": [
        "compareorder"
      ]
    },
    {
      "page": "condense.scantwo",
      "title": "Condense the output from a 2-d genome scan",
      "topics": [
        "condense.scantwo"
      ]
    },
    {
      "page": "convert.map",
      "title": "Change map function for a genetic map",
      "topics": [
        "convert.map"
      ]
    },
    {
      "page": "convert.scanone",
      "title": "Convert output from scanone for R/qtl version 0.98",
      "topics": [
        "convert.scanone"
      ]
    },
    {
      "page": "convert.scantwo",
      "title": "Convert output from scantwo for R/qtl version 1.03 and earlier",
      "topics": [
        "convert.scantwo"
      ]
    },
    {
      "page": "convert2riself",
      "title": "Convert a cross to RIL by selfing",
      "topics": [
        "convert2riself"
      ]
    },
    {
      "page": "convert2risib",
      "title": "Convert a cross to RIL by sib mating",
      "topics": [
        "convert2risib"
      ]
    },
    {
      "page": "convert2sa",
      "title": "Convert a sex-specific map to a sex-averaged one",
      "topics": [
        "convert2sa"
      ]
    },
    {
      "page": "countXO",
      "title": "Count number of obligate crossovers for each individual",
      "topics": [
        "countXO"
      ]
    },
    {
      "page": "drop.dupmarkers",
      "title": "Drop duplicate markers",
      "topics": [
        "drop.dupmarkers"
      ]
    },
    {
      "page": "drop.markers",
      "title": "Drop a set of markers",
      "topics": [
        "drop.markers"
      ]
    },
    {
      "page": "drop.nullmarkers",
      "title": "Drop markers without any genotype data",
      "topics": [
        "drop.nullmarkers"
      ]
    },
    {
      "page": "dropfromqtl",
      "title": "Drop a QTL from a qtl object",
      "topics": [
        "dropfromqtl"
      ]
    },
    {
      "page": "droponemarker",
      "title": "Drop one marker at a time and determine effect on genetic map",
      "topics": [
        "droponemarker"
      ]
    },
    {
      "page": "effectplot",
      "title": "Plot phenotype means against genotypes at one or two markers",
      "topics": [
        "effectplot"
      ]
    },
    {
      "page": "effectscan",
      "title": "Plot estimated QTL effects across the whole genome",
      "topics": [
        "effectscan"
      ]
    },
    {
      "page": "est.map",
      "title": "Estimate genetic maps",
      "topics": [
        "est.map"
      ]
    },
    {
      "page": "est.rf",
      "title": "Estimate pairwise recombination fractions",
      "topics": [
        "est.rf"
      ]
    },
    {
      "page": "fake.4way",
      "title": "Simulated data for a 4-way cross",
      "topics": [
        "fake.4way"
      ]
    },
    {
      "page": "fake.bc",
      "title": "Simulated data for a backcross",
      "topics": [
        "fake.bc"
      ]
    },
    {
      "page": "fake.f2",
      "title": "Simulated data for an F2 intercross",
      "topics": [
        "fake.f2"
      ]
    },
    {
      "page": "fill.geno",
      "title": "Fill holes in genotype data",
      "topics": [
        "fill.geno"
      ]
    },
    {
      "page": "find_large_intervals",
      "title": "Find large intervals in a map",
      "topics": [
        "find_large_intervals"
      ]
    },
    {
      "page": "find.flanking",
      "title": "Find flanking markers for a specified position",
      "topics": [
        "find.flanking"
      ]
    },
    {
      "page": "find.marker",
      "title": "Find marker closest to a specified position",
      "topics": [
        "find.marker"
      ]
    },
    {
      "page": "findmarkerindex",
      "title": "Determine the numeric index for a marker",
      "topics": [
        "find.markerindex"
      ]
    },
    {
      "page": "find.markerpos",
      "title": "Find position of a marker",
      "topics": [
        "find.markerpos"
      ]
    },
    {
      "page": "find.pheno",
      "title": "Find column number for a particular phenotype",
      "topics": [
        "find.pheno"
      ]
    },
    {
      "page": "find.pseudomarker",
      "title": "Find the pseudomarker closest to a specified position",
      "topics": [
        "find.pseudomarker"
      ]
    },
    {
      "page": "findDupMarkers",
      "title": "Find markers with identical genotype data",
      "topics": [
        "findDupMarkers"
      ]
    },
    {
      "page": "fitqtl",
      "title": "Fit a multiple-QTL model",
      "topics": [
        "fitqtl"
      ]
    },
    {
      "page": "fitstahl",
      "title": "Fit Stahl interference model",
      "topics": [
        "fitstahl"
      ]
    },
    {
      "page": "flip.order",
      "title": "Flip the orders of markers on a set of chromosomes",
      "topics": [
        "flip.order"
      ]
    },
    {
      "page": "formLinkageGroups",
      "title": "Partition markers into linkage groups",
      "topics": [
        "formLinkageGroups"
      ]
    },
    {
      "page": "formMarkerCovar",
      "title": "Create matrix of marker covariates for QTL analysis",
      "topics": [
        "formMarkerCovar"
      ]
    },
    {
      "page": "geno.crosstab",
      "title": "Create table of two-locus genotypes",
      "topics": [
        "geno.crosstab"
      ]
    },
    {
      "page": "geno.image",
      "title": "Plot grid of genotype data",
      "topics": [
        "geno.image"
      ]
    },
    {
      "page": "geno.table",
      "title": "Create table of genotype distributions",
      "topics": [
        "geno.table"
      ]
    },
    {
      "page": "getid",
      "title": "Pull out the individual identifiers from a cross",
      "topics": [
        "getid"
      ]
    },
    {
      "page": "groupclusteredheatmap",
      "title": "Retrieving groups of traits after clustering",
      "topics": [
        "groupclusteredheatmap"
      ]
    },
    {
      "page": "hyper",
      "title": "Data on hypertension",
      "topics": [
        "hyper"
      ]
    },
    {
      "page": "inferFounderHap",
      "title": "Crude reconstruction of founder haplotypes in multi-parent RIL",
      "topics": [
        "inferFounderHap"
      ]
    },
    {
      "page": "inferredpartitions",
      "title": "Identify inferred partitions in mapping QTL to a phylogenetic tree",
      "topics": [
        "inferredpartitions"
      ]
    },
    {
      "page": "interpPositions",
      "title": "Interpolate positions from one map to another",
      "topics": [
        "interpPositions"
      ]
    },
    {
      "page": "jittermap",
      "title": "Jitter marker positions in a genetic map",
      "topics": [
        "jittermap"
      ]
    },
    {
      "page": "listeria",
      "title": "Data on Listeria monocytogenes susceptibility",
      "topics": [
        "listeria"
      ]
    },
    {
      "page": "locateXO",
      "title": "Estimate locations of crossovers",
      "topics": [
        "locateXO"
      ]
    },
    {
      "page": "locations",
      "title": "Genetic locations of traits for the multitrait dataset",
      "topics": [
        "locations"
      ]
    },
    {
      "page": "lodint",
      "title": "LOD support interval",
      "topics": [
        "lodint"
      ]
    },
    {
      "page": "makeqtl",
      "title": "Make a qtl object",
      "topics": [
        "makeqtl"
      ]
    },
    {
      "page": "map10",
      "title": "An example genetic map",
      "topics": [
        "map10"
      ]
    },
    {
      "page": "map2table",
      "title": "Convert genetic map from list to table.",
      "topics": [
        "map2table"
      ]
    },
    {
      "page": "mapthis",
      "title": "Simulated data for illustrating genetic map construction",
      "topics": [
        "mapthis"
      ]
    },
    {
      "page": "markerlrt",
      "title": "General likelihood ratio test for association between marker pairs",
      "topics": [
        "markerlrt"
      ]
    },
    {
      "page": "markernames",
      "title": "Pull out the marker names from a cross",
      "topics": [
        "markernames"
      ]
    },
    {
      "page": "max.scanone",
      "title": "Maximum peak in genome scan",
      "topics": [
        "max.scanone"
      ]
    },
    {
      "page": "max.scanPhyloQTL",
      "title": "Maximum peak in genome scan to map a QTL to a phylogenetic tree",
      "topics": [
        "max.scanPhyloQTL"
      ]
    },
    {
      "page": "max.scantwo",
      "title": "Maximum peak in two-dimensional genome scan",
      "topics": [
        "max.scantwo"
      ]
    },
    {
      "page": "movemarker",
      "title": "Move a marker to a new chromosome",
      "topics": [
        "movemarker"
      ]
    },
    {
      "page": "MQM",
      "title": "Introduction to Multiple QTL Model (MQM) mapping",
      "topics": [
        "MQM"
      ]
    },
    {
      "page": "mqmaugment",
      "title": "MQM augmentation",
      "topics": [
        "mqmaugment"
      ]
    },
    {
      "page": "mqmautocofactors",
      "title": "Automatic setting of cofactors, taking marker density into account",
      "topics": [
        "mqmautocofactors"
      ]
    },
    {
      "page": "mqmextractmarkers",
      "title": "MQM marker extraction",
      "topics": [
        "mqmextractmarkers"
      ]
    },
    {
      "page": "mqmfind.marker",
      "title": "Fetch significant markers after permutation analysis",
      "topics": [
        "mqmfind.marker"
      ]
    },
    {
      "page": "mqmgetmodel",
      "title": "Retrieve the QTL model used in mapping from the results of an MQM scan",
      "topics": [
        "mqmgetmodel"
      ]
    },
    {
      "page": "mqmpermutation",
      "title": "Estimate QTL LOD score significance using permutations or simulations",
      "topics": [
        "mqmpermutation"
      ]
    },
    {
      "page": "mqmplotcircle",
      "title": "Circular genome plot for MQM",
      "topics": [
        "mqmplot.circle"
      ]
    },
    {
      "page": "mqmplotcistrans",
      "title": "cis-trans plot",
      "topics": [
        "mqmplot.cistrans"
      ]
    },
    {
      "page": "mqmplotclusteredheatmap",
      "title": "Plot clustered heatmap of MQM scan on multiple phenotypes",
      "topics": [
        "mqmplot.clusteredheatmap"
      ]
    },
    {
      "page": "mqmplotcofactors",
      "title": "Plot cofactors on the genetic map",
      "topics": [
        "mqmplot.cofactors"
      ]
    },
    {
      "page": "mqmplotdirectedqtl",
      "title": "Plot LOD*Effect curves of a multiple-QTL model",
      "topics": [
        "mqmplot.directedqtl"
      ]
    },
    {
      "page": "mqmplotheatmap",
      "title": "Heatmap of a genome of MQM scan on multiple phenotypes",
      "topics": [
        "mqmplot.heatmap"
      ]
    },
    {
      "page": "mqmplotmultitrait",
      "title": "Plot the results from a genomescan using a multiple-QTL model on multiple phenotypes",
      "topics": [
        "mqmplot.multitrait"
      ]
    },
    {
      "page": "mqmplotpermutations",
      "title": "Plot results from mqmpermutation",
      "topics": [
        "mqmplot.permutations"
      ]
    },
    {
      "page": "mqmplotsingletrait",
      "title": "Plot LOD curves of a multiple-QTL model",
      "topics": [
        "mqmplot.singletrait"
      ]
    },
    {
      "page": "mqmprocesspermutation",
      "title": "Convert mqmmulti objects into a scanoneperm object",
      "topics": [
        "mqmprocesspermutation"
      ]
    },
    {
      "page": "mqmscan",
      "title": "Genome scan with a multiple QTL model (MQM)",
      "topics": [
        "mqmscan"
      ]
    },
    {
      "page": "mqmscanall",
      "title": "Parallelized MQM on multiple phenotypes in a cross object",
      "topics": [
        "mqmscanall"
      ]
    },
    {
      "page": "mqmscanfdr",
      "title": "Estimate FDR for multiple trait QTL analysis",
      "topics": [
        "mqmscanfdr"
      ]
    },
    {
      "page": "mqmsetcofactors",
      "title": "Set cofactors at fixed intervals, to be used with MQM",
      "topics": [
        "mqmsetcofactors"
      ]
    },
    {
      "page": "mqmtestnormal",
      "title": "Shapiro normality test used for MQM",
      "topics": [
        "mqmtestnormal"
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    },
    {
      "page": "multitrait",
      "title": "Example Cross object from R/QTL with multiple traits",
      "topics": [
        "multitrait"
      ]
    },
    {
      "page": "nchr",
      "title": "Determine the number of chromosomes",
      "topics": [
        "nchr"
      ]
    },
    {
      "page": "nind",
      "title": "Determine the number of individuals QTL experiment",
      "topics": [
        "nind"
      ]
    },
    {
      "page": "nmar",
      "title": "Determine the numbers of markers on each chromosome",
      "topics": [
        "nmar"
      ]
    },
    {
      "page": "nmissing",
      "title": "Number of missing genotypes",
      "topics": [
        "nmissing"
      ]
    },
    {
      "page": "nphe",
      "title": "Determine the number of phenotypes QTL experiment",
      "topics": [
        "nphe"
      ]
    },
    {
      "page": "nqrank",
      "title": "Transform a vector of quantitative values to the corresponding normal quantiles",
      "topics": [
        "nqrank"
      ]
    },
    {
      "page": "nqtl",
      "title": "Determine the number of QTL in a QTL object",
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        "nqtl"
      ]
    },
    {
      "page": "ntyped",
      "title": "Number of genotypes",
      "topics": [
        "ntyped"
      ]
    },
    {
      "page": "nullmarkers",
      "title": "Identify markers without any genotype data",
      "topics": [
        "nullmarkers"
      ]
    },
    {
      "page": "orderMarkers",
      "title": "Find an initial order for markers within chromosomes",
      "topics": [
        "orderMarkers"
      ]
    },
    {
      "page": "phenames",
      "title": "Pull out the phenotypes names from a cross",
      "topics": [
        "phenames"
      ]
    },
    {
      "page": "pickMarkerSubset",
      "title": "Identify the largest subset of markers that are some distance apart",
      "topics": [
        "pickMarkerSubset"
      ]
    },
    {
      "page": "plot.comparegeno",
      "title": "Plot genotype comparison",
      "topics": [
        "plot.comparegeno"
      ]
    },
    {
      "page": "plot.cross",
      "title": "Plot various features of a cross object",
      "topics": [
        "plot.cross"
      ]
    },
    {
      "page": "plot.qtl",
      "title": "Plot QTL locations",
      "topics": [
        "plot.qtl"
      ]
    },
    {
      "page": "plot.rfmatrix",
      "title": "Plot recombination fractions or LOD scores for a single marker",
      "topics": [
        "plot.rfmatrix"
      ]
    },
    {
      "page": "plot.scanone",
      "title": "Plot LOD curves",
      "topics": [
        "plot.scanone"
      ]
    },
    {
      "page": "plot.scanoneboot",
      "title": "Plot results of bootstrap for QTL position",
      "topics": [
        "plot.scanoneboot"
      ]
    },
    {
      "page": "plot.scanoneperm",
      "title": "Plot permutation results for a single-QTL genome scan",
      "topics": [
        "plot.scanoneperm"
      ]
    },
    {
      "page": "plot.scanPhyloQTL",
      "title": "Plot LOD curves from single-QTL scan to map QTL to a phylogenetic tree",
      "topics": [
        "plot.scanPhyloQTL"
      ]
    },
    {
      "page": "plot.scantwo",
      "title": "Plot LOD scores for a two-dimensional genome scan",
      "topics": [
        "plot.scantwo"
      ]
    },
    {
      "page": "plot.scantwoperm",
      "title": "Plot permutation results for a 2d, 2-QTL genome scan",
      "topics": [
        "plot.scantwoperm"
      ]
    },
    {
      "page": "plot.errorlod",
      "title": "Plot grid of error LOD values",
      "topics": [
        "plotErrorlod"
      ]
    },
    {
      "page": "plot.geno",
      "title": "Plot observed genotypes, flagging likely errors",
      "topics": [
        "plotGeno"
      ]
    },
    {
      "page": "plot.info",
      "title": "Plot the proportion of missing genotype information",
      "topics": [
        "plotInfo"
      ]
    },
    {
      "page": "plotLodProfile",
      "title": "Plot 1-d LOD profiles for a multiple QTL model",
      "topics": [
        "plotLodProfile"
      ]
    },
    {
      "page": "plot.map",
      "title": "Plot genetic map",
      "topics": [
        "plot.map",
        "plotMap"
      ]
    },
    {
      "page": "plot.missing",
      "title": "Plot grid of missing genotypes",
      "topics": [
        "plotMissing"
      ]
    },
    {
      "page": "plotModel",
      "title": "Plot a QTL model",
      "topics": [
        "plotModel"
      ]
    },
    {
      "page": "plot.pheno",
      "title": "Plot a phenotype distribution",
      "topics": [
        "plotPheno"
      ]
    },
    {
      "page": "plot.pxg",
      "title": "Plot phenotypes versus marker genotypes",
      "topics": [
        "plotPXG"
      ]
    },
    {
      "page": "plot.rf",
      "title": "Plot recombination fractions",
      "topics": [
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      ]
    },
    {
      "page": "pull.argmaxgeno",
      "title": "Pull out the results of the Viterbi algorithm from a cross",
      "topics": [
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    },
    {
      "page": "pull.draws",
      "title": "Pull out the genotype imputations from a cross",
      "topics": [
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    },
    {
      "page": "pull.geno",
      "title": "Pull out the genotype data from a cross",
      "topics": [
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    },
    {
      "page": "pull.genoprob",
      "title": "Pull out the genotype probabilities from a cross",
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    },
    {
      "page": "pull.map",
      "title": "Pull out the genetic map from a cross",
      "topics": [
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    },
    {
      "page": "pull.markers",
      "title": "Drop all but a selected set of markers",
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    },
    {
      "page": "pull.pheno",
      "title": "Pull out phenotype data from a cross",
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    },
    {
      "page": "pull.rf",
      "title": "Pull out recombination fractions or LOD scores from a cross object",
      "topics": [
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    },
    {
      "page": "qtlversion",
      "title": "Installed version of R/qtl",
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    },
    {
      "page": "read.cross",
      "title": "Read data for a QTL experiment",
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    {
      "page": "readMWril",
      "title": "Read data for 4- or 8-way RIL",
      "topics": [
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    },
    {
      "page": "reduce2grid",
      "title": "Reduce to a grid of pseudomarkers.",
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    {
      "page": "refineqtl",
      "title": "Refine the positions of QTL",
      "topics": [
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    },
    {
      "page": "reorderqtl",
      "title": "Reorder the QTL in a qtl object",
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    {
      "page": "replace.map",
      "title": "Replace the genetic map of a cross",
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    },
    {
      "page": "replacemap.scanone",
      "title": "Replace the genetic map in QTL mapping results with an alternate map",
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      "title": "Replace the genetic map in QTL mapping results with an alternate map",
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    {
      "page": "replaceqtl",
      "title": "Replace a QTL in a qtl object with a different position",
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    {
      "page": "rescalemap",
      "title": "Rescale genetic maps",
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    {
      "page": "ripple",
      "title": "Compare marker orders",
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    {
      "page": "scanone",
      "title": "Genome scan with a single QTL model",
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    {
      "page": "scanoneboot",
      "title": "Bootstrap to get interval estimate of QTL location",
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    {
      "page": "scanonevar",
      "title": "Genome scan for QTL affecting mean and/or variance",
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      "page": "scanonevar.meanperm",
      "title": "Permutation test for mean effect in scanonevar",
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      "title": "Permutation test for variance effect in scanonevar",
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    {
      "page": "scanPhyloQTL",
      "title": "Single-QTL genome scan to map QTL to a phylogenetic tree",
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    {
      "page": "scanqtl",
      "title": "General QTL scan",
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      "page": "scantwo",
      "title": "Two-dimensional genome scan with a two-QTL model",
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    {
      "page": "scantwopermhk",
      "title": "Permutation test for 2d genome scan by Haley-Knott regression",
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      "page": "shiftmap",
      "title": "Shift starting points in genetic maps",
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      "page": "sim.cross",
      "title": "Simulate a QTL experiment",
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      "title": "Simulate genotypes given observed marker data",
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      "title": "Simulate a genetic map",
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      "title": "Strip partially informative genotypes",
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      "title": "Subsetting data for QTL experiment",
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      "title": "Subsetting chromosomes for a genetic map",
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        "[.map"
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      "page": "subset.scanone",
      "title": "Subsetting the results of a genome scan",
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      "page": "subset.scanoneperm",
      "title": "Subsetting permutation test results",
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      "title": "Subsetting the results of a 2-d genome scan",
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      "page": "subset.scantwoperm",
      "title": "Subsetting two-dimensional permutation test results",
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      "page": "summary.comparegeno",
      "title": "Print pairs of individuals with similar genotype data.",
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    {
      "page": "summary.cross",
      "title": "Print summary of QTL experiment",
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      "title": "Summary of fit of qtl model",
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      "title": "Print summary of a QTL object",
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      "title": "Print summary of ripple results",
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      "title": "Summarize the results of a genome scans",
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      "title": "Bootstrap confidence interval for QTL location",
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      "title": "LOD thresholds from scanone permutation results",
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      "title": "Summarize the results a genome scan to map a QTL to a phylogenetic tree",
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      "title": "Summarize the results of a two-dimensional genome scan",
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      "title": "LOD thresholds from scantwo permutation results",
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      "title": "Print summary of a genetic map",
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