Collaborative Cross colors
Calculate genotype frequencies
Batch columns by pattern of missing values
Add thresholds to genome scan plot
Calculate conditional genotype probabilities
Calculate genotyping error LOD scores
Calculate entropy of genotype probability distribution
Basic summaries of a cross2 object
Split vector into batches
Calculate Bayes credible intervals
Calculate kinship matrix
Calculate founder minor allele frequencies from raw SNP genotypes
Join viterbi results for different chromosomes
Calculate strain distribution pattern from SNP genotypes
Calculate minor allele frequency from raw SNP genotypes
Combine columns from multiple scan1 permutation results
Calculate indicators of which marker/pseudomarker positions are along a fixed grid
Join genotype imputations for different chromosomes
Calculate heterozygosities
Combine matrices by columns, expanding and aligning rows
Chi-square test on all pairs of columns
Count numbers of crossovers
Check a cross2 object
Create a function to query genes
Compare individuals' genotype data
Compare two sets of genotype probabilities
Join genome scan results for different phenotypes.
Join genotype probabilities for different chromosomes
Clean genotype probabilities
Clean scan1 output
Create snp information table for a cross
Drop markers with no genotype data
Estimate heritability with a linear mixed model
Find gaps in a genetic map
Find name of indexed snp
Calculate eigen decomposition of kinship matrix
create_variant_query_func
Create a function to query variants
Calculate estimated heterozygosity from raw SNP genotypes
Calculate genotype frequencies from raw SNP genotypes
Find markers by chromosome position
Find positions of markers
Drop markers from a cross2 object
Overall maximum LOD score
Insert pseudomarkers into a marker map
Interpolate genotype probabilities
Interpolate between maps
Calculate SNP genotype matrix from strain distribution patterns
Calculate chromosome lengths
Guess phase of imputed genotypes
Find peaks in a set of LOD curves
Create index of equivalent SNPs
Find genotypes with maximum marginal probabilities
Get X chromosome covariates
Calculate LOD support intervals
Locate crossovers
Get common set of IDs from objects
Recode SNPs by major allele
Read phenotype data
Fit single-QTL model at a single position
Define strata based on rows of a matrix
Subset a map to positions on a grid
Find pair with most similar genotypes
Find position with maximum LOD score
Plot QTL peak locations
Plot phenotype vs genotype
Predict SNP genotypes
Plot SNP associations
Plot a genome scan
Replace individual IDs
Pull genotype probabilities for an interval
Print a cross2 object
Clean an object
Compare two marker maps
Scale kinship matrix
Basic summary of compare_geno object
Permutation test for genome scan with a single-QTL model
Convert strain distribution patterns to character strings
Single-QTL genome scan at imputed SNPs
Simulate genotypes given observed marker data
Summarize scan1perm results
Maximum LOD score from genome scan with a single-QTL model
Calculate QTL effects in scan along one chromosome
Combine data from scan1perm objects
Pull genotype probabilities for a particular position
Join genotype imputations for different individuals
Subsetting imputed genotypes
Plot genotype probabilities for one individual on one chromosome.
Estimate genetic maps
Convert R/qtl cross object to new format
Plot of compare_geno object.
Plot comparison of two sets of genotype probabilities
qtl2: Quantitative Trait Locus Mapping in Experimental Crosses
Convert genotype probabilities to allele probabilities
Count missing genotypes
Find IBD segments for a set of strains
Plot QTL effects along chromosome
Convert genotype probabilities to SNP probabilities
Plot LOD scores vs QTL peak locations
Plot gene locations for a genomic interval
Join genotype probabilities for different individuals
Installed version of R/qtl2
Join genome scan results for different chromosomes.
Genome scan with a single-QTL model
Subsetting Viterbi results
Calculate BLUPs of QTL effects in scan along one chromosome
Subset genotype probability array to pseudomarkers on a grid
Read a csv file
Print summary of scan1perm permutations
Create table of top snp associations
Calculate most probable sequence of genotypes
Subset scan1 output
Reduce the lengths of gaps in a map
Reduce markers to a subset of more-evenly-spaced ones
Read a csv file that has numeric columns
Plot one individual's genome-wide genotypes
Internal functions
Drop all but a specified set of markers
Join Viterbi results for different individuals
Subsetting genotype probabilities
Read QTL data from files
Summary of cross2 object
Zip a set of data files
Write a control file for QTL data
Get x-axis position for genomic location
Subsetting data for a QTL experiment