File: INDEX

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qtl 1.08-56-1
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+.scanone               Arithmetic Operators for scanone and scantwo
                        results
+.scanoneperm           Arithmetic Operators for permutation results
add.cim.covar           Indicate marker covariates from composite
                        interval mapping
add.threshold           Add significance threshold to plot
addint                  Add pairwise interaction to a multiple-QTL
                        model
addpair                 Scan for an additional pair of QTL in a
                        multiple-QTL model
addqtl                  Scan for an additional QTL in a multiple-QTL
                        model
addtoqtl                Add to a qtl object
argmax.geno             Reconstruct underlying genotypes
badorder                An intercross with misplaced markers
bayesint                Bayesian credible interval
bristle3                Data on bristle number in Drosophila
bristleX                Data on bristle number in Drosophila
c.cross                 Combine data for QTL experiments
c.scanone               Combine columns from multiple scanone results
c.scanoneperm           Combine data from scanone permutations
c.scantwoperm           Combine data from scantwo permutations
calc.errorlod           Identify likely genotyping errors
calc.genoprob           Calculate conditional genotype probabilities
cbind.scanoneperm       Combine columns from multiple scanone
                        permutation results
checkAlleles            Identify markers with switched alleles
chrlen                  Chromosome lengths in QTL experiment
cim                     Composite interval mapping
clean.cross             Remove derived data
clean.scantwo           Clean up scantwo output
comparecrosses          Compare two cross objects.
comparegeno             Compare individuals' genotype data
compareorder            Compare two orderings of markers on a
                        chromosome
condense.scantwo        Condense the output from a 2-d genome scan
convert.scanone         Convert output from scanone for R/qtl version
                        0.98
convert.scantwo         Convert output from scantwo for R/qtl version
                        1.03 and earlier
countXO                 Count number of obligate crossovers for each
                        individual
drop.markers            Drop a set of markers
drop.nullmarkers        Drop markers without any genotype data
dropfromqtl             Drop a QTL from a qtl object
effectplot              Plot phenotype means against genotypes at one
                        or two markers.
effectscan              Plot estimated QTL effects across the whole
                        genome
est.map                 Estimate genetic maps
est.rf                  Estimate pairwise recombination fractions
fake.4way               Simulated data for a 4-way cross
fake.bc                 Simulated data for a backcross
fake.f2                 Simulated data for an F2 intercross
fill.geno               Fill holes in genotype data
find.flanking           Find flanking markers for a specified position
find.marker             Find marker closest to a specified position
find.markerpos          Find position of a marker.
find.pheno              Find column number for a particular phenotype.
find.pseudomarker       Find the pseudomarker closest to a specified
                        position
fitqtl                  Fit a multiple-QTL model
fitstahl                Fit Stahl interference model
geno.crosstab           Create table of two-locus genotypes
geno.image              Plot grid of genotype data
geno.table              Create table of genotype distributions
hyper                   Data on hypertension
jittermap               Jitter marker positions in a genetic map
listeria                Data on Listeria monocytogenes susceptibility
lodint                  LOD support interval
makeqtl                 Make a qtl object
map10                   An example genetic map
max.scanone             Maximum peak in genome scan
max.scantwo             Maximum peak in two-dimensional genome scan
movemarker              Move a marker to a new chromosome
nmissing                Number of missing genotypes
plot.cross              Plot various features of a cross object
plot.errorlod           Plot grid of error LOD values
plot.geno               Plot observed genotypes, flagging likely errors
plot.info               Plot the proportion of missing genotype
                        information
plot.map                Plot genetic map
plot.missing            Plot grid of missing genotypes
plot.pheno              Plot a phenotype distribution
plot.pxg                Plot phenotypes versus marker genotypes.
plot.qtl                Plot QTL locations
plot.rf                 Plot recombination fractions
plot.scanone            Plot LOD curves
plot.scanoneboot        Plot results of bootstrap for QTL position.
plot.scanoneperm        Plot permutation results for a single-QTL
                        genome scan
plot.scantwo            Plot LOD scores for a two-dimensional genome
                        scan
plot.scantwoperm        Plot permutation results for a 2d, 2-QTL genome
                        scan
plotLodProfile          Plot 1-d LOD profiles for a multiple QTL model
pull.geno               Pull out the genotype data from a cross
pull.map                Pull out the genetic map from a cross
pull.pheno              Pull out phenotype data from a cross
qtl-package             Introductory comments on R/qtl
qtlversion              Installed version of R/qtl
read.cross              Read data for a QTL experiment
refineqtl               Refine the positions of QTL
reorderqtl              Reorder the QTL in a qtl object.
replace.map             Replace the genetic map of a cross
replaceqtl              Replace a QTL in a qtl object with a different
                        position.
ripple                  Compare marker orders
scanone                 Genome scan with a single QTL model
scanoneboot             Bootstrap to get interval estimate of QTL
                        location
scanqtl                 General QTL scan
scantwo                 Two-dimensional genome scan with a two-QTL
                        model
sim.cross               Simulate a QTL experiment
sim.geno                Simulate genotypes given observed marker data
sim.map                 Simulate a genetic map
strip.partials          Strip partially informative genotypes
subset.cross            Subsetting data for QTL experiment
subset.scanone          Subsetting the results of a genome scan
subset.scantwo          Subsetting the results of a 2-d genome scan
summary.cross           Print summary of QTL experiment
summary.fitqtl          Summary of fit of qtl model
summary.map             Print summary of a genetic map
summary.qtl             Print summary of a QTL object
summary.ripple          Print summary of ripple results
summary.scanone         Summarize the results of a genome scans
summary.scanoneboot     Bootstrap confidence interval for QTL location
summary.scanoneperm     LOD thresholds from scanone permutation results
summary.scantwo         Summarize the results of a two-dimensional
                        genome scan
summary.scantwo.old     Summarize the results of a two-dimensional
                        genome scan
summary.scantwoperm     LOD thresholds from scantwo permutation results
switch.order            Switch the order of markers on a chromosome
top.errorlod            List genotypes with large error LOD scores
tryallpositions         Test all possible positions for a marker
write.cross             Write data for a QTL experiment to a file