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JM4QTN: Joint Mapping for Quantitative Trait Loci

Overview

JM4QTN supports joint mapping and related analyses for quantitative trait loci (QTL). The package provides phenotype summaries, genotype probability and imputation (association vs linkage mapping), permutation-based thresholds with stepwise regression (via StepReg), and scan statistics comparing full vs reduced linear models (joint_map).

Key Features

Core analysis

Permutation testing (permutation_test) for empirical p-value and LOD cutoffs under stepwise selection
Skeleton model (skeleton_build / skeletion_build) fitting the selected model using those cutoffs
Joint mapping scan (joint_map) over candidate terms vs the skeleton model

Genotypes and map

Genotype probabilities / imputation (genotype_prob) for AM or LM, optional virtual markers
Expected genotype distribution (expected_genotype_dist) and genotype frequencies (genotype_freq)
Haldane map (haldane_map) for recombination

Phenotypes

Phenotype statistics (pheno_stats): normality, ANOVA, least squares means (via lsmeans)

Installation

# Install from GitHub
if (!require("devtools")) install.packages("devtools")
devtools::install_github("JunhuiLi1017/JM4QTN")

## or install from CRAN
install.pakcages("JM4QTN")

# Load the package
library(JM4QTN)

Quick start

1. Phenotype analysis (`pheno_stats`)

Designed for multi-environment trials: columns E, B, R, G, then traits.

pheno_data <- data.frame(
  E = rep(c("Env1", "Env2"), each = 60),
  B = rep(c("B1", "B2"), each = 30, times = 2),
  R = rep(1:5, 24),
  G = factor(rep(1:12, 10)),
  Height = rnorm(120, 175, 8),
  Weight = rnorm(120, 75, 12)
)

results <- pheno_stats(pheno_data)
results$Height$normality_test
results$Height$ANOVA
results$Height$lsmeans

2. Genotype probabilities (`genotype_prob`)

genetic_map <- data.frame(
  marker = c("M1", "M2", "M3"),
  chr = c(1, 1, 1),
  pos = c(0, 10, 20)
)
geno_data <- matrix(sample(0:2, 15, TRUE), nrow = 5, ncol = 3,
                    dimnames = list(paste0("Ind", 1:5), c("M1", "M2", "M3")))

result_am <- genotype_prob(genetic_map, geno_data, method = "AM")
result_lm <- genotype_prob(genetic_map, geno_data, method = "LM",
                           croType = "F2", steps = 0)

3. Permutation thresholds, skeleton model, and joint mapping

Formula-based workflow with genotype columns bound into data (see package examples for joint_map).

pheno_data <- data.frame(
  Trait1 = rnorm(100, 100, 15),
  Trait2 = rnorm(100, 50, 8),
  Popu = rep(c("Pop1", "Pop2"), each = 50)
)
geno_data <- matrix(sample(0:2, 100 * 50, TRUE), nrow = 100, ncol = 50)
colnames(geno_data) <- paste0("M", 1:50)
data1 <- cbind(pheno_data, geno_data)

terms <- c("Popu", paste0(colnames(geno_data), ":Popu"))
formula1 <- reformulate(terms, response = "Trait1")

cut_off_list <- permutation_test(formula1, data1, n = 100, alpha = 0.1)

skeleton <- skeleton_build(
  formula1, data1,
  strategy = "bidirection", metric = "SL",
  cut_off_list = cut_off_list
)

results <- joint_map(
  formula1, data1, skeleton,
  include = "Popu", cut_off_list = cut_off_list
)
results$p_value
results$lod

4. Supporting utilities

haldane_map(0.1)   # genetic distance (Morgan) -> recombination fraction
genotype_freq("Fn", generation = 3, genotype_index = 1, recomb_aq = 0.1, recomb_qb = 0.2)
expected_genotype_dist("22", "F2", Gn = 2, x = 0.1, y = 0.2)

Function reference (exported)

Function	Description
`joint_map()`	Compare candidate model terms to a fitted skeleton; returns p-values and LOD-like statistics
`permutation_test()`	Permutation distribution and empirical cutoffs for stepwise linear models
`skeleton_build()`	Alias for `skeletion_build()` (preferred spelling)
`skeletion_build()`	Fit stepwise skeleton using permutation p-value as StepReg entry/stay levels
`genotype_prob()`	Genotype probabilities / imputation (AM or LM)
`genotype_freq()`	Genotype class frequencies by cross type and generation
`expected_genotype_dist()`	Expected genotype distribution by marker pattern and cross
`haldane_map()`	Haldane mapping function
`pheno_stats()`	Normality tests, ANOVA, lsmeans for structured phenotype tables

Backward-compatible names (same package, alternate spelling): calculate_genotype_frequencies, calculate_expected_genotype_distribution, haldane_mapping_function — see individual help pages.

Data notes

pheno_stats: expects E, B, R, G as the first four columns, then traits.
genotype_prob: rows = individuals, columns = markers; column order must align with GeneticMap rows.
joint_map / permutation_test: supply a single data frame containing phenotypes, population, and numeric genotype columns used in the formula.

Citation

@Manual{JM4QTN,
  title = {JM4QTN: Joint Mapping for Quantitative Trait Loci},
  author = {Junhui Li and Wenxin Liu},
  year = {2026},
  note = {R package version 1.0.0},
  url = {https://github.com/JunhuiLi1017/JM4QTN}
}

References

Jiang, C. and Zeng, Z.B. (1995). Multiple trait analysis of genetic mapping for quantitative trait loci. Genetics, 140(3), 1111-1127.
Churchill, G.A. and Doerge, R.W. (1994). Empirical threshold values for quantitative trait mapping. Genetics, 138(3), 963-971.
Haldane, J.B.S. (1919). The combination of linkage values and the calculation of distances between the loci of linked factors. Journal of Genetics, 8(3), 299-309.

Contributing

Issues and pull requests are welcome on GitHub.

License

This project is licensed under the GNU General Public License v2.0 - see the GNU GPLv2 license text for details.

Contact

Maintainer: Junhui Li junhuili@cau.edu.cn
GitHub: https://github.com/JunhuiLi1017/JM4QTN

These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
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