CRAN/E | dQTG.seq

dQTG.seq

A BSA Software for Detecting All Types of QTLs in BC, DH, RIL and F2

Installation

About

The new (dQTG.seq1 and dQTG.seq2) and existing (SmoothLOD, G', deltaSNP and ED) bulked segregant analysis methods are used to identify various types of quantitative trait loci for complex traits via extreme phenotype individuals in bi-parental segregation populations (F2, backcross, doubled haploid and recombinant inbred line). The numbers of marker alleles in extreme low and high pools are used in existing methods to identify trait-related genes, while the numbers of marker alleles and genotypes in extreme low and high pools are used in the new methods to construct a new statistic Gw for identifying trait-related genes. dQTG-seq2 is feasible to identify extremely over-dominant and small-effect genes in F2. Li P, Li G, Zhang YW, Zuo JF, Liu JY, Zhang YM (2022, doi:10.1016/j.xplc.2022.100319).

Key Metrics

Version 1.0.2
R ≥ 3.5.0
Published 2023-03-22 408 days ago
Needs compilation? no
License GPL-2
License GPL-3
CRAN checks dQTG.seq results

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Maintainer

Maintainer

Yuan-Ming Zhang

soyzhang@mail.hzau.edu.cn

Authors

Pei Li

aut

Yuan-Ming Zhang

aut / cre

Contacts

Yuan-Ming Zhang

Material

Reference manual
Package source

macOS

r-release

arm64

r-oldrel

arm64

r-release

x86_64

r-oldrel

x86_64

Windows

r-devel

x86_64

r-release

x86_64

r-oldrel

x86_64

Old Sources

dQTG.seq archive

Depends

R ≥ 3.5.0

Imports

BB
data.table
doParallel
openxlsx
qtl
stringr
writexl
vroom
parallel
foreach