Joint Mapping for Quantitative Trait Loci.
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 withGeneticMaprows.joint_map/permutation_test: supply a singledataframe 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 [email protected]
- GitHub: https://github.com/JunhuiLi1017/JM4QTN.