Related Experiment Video
Updated: Feb 7, 2026

08:38
Targeted DNA Methylation Analysis by Next-generation Sequencing
Published on: February 24, 2015
38.0K
QTLseqr: An R Package for Bulk Segregant Analysis with Next-Generation Sequencing.
The Plant Genome
|July 20, 2018
Summary
Next-Generation Sequencing Bulk Segregant Analysis (NGS-BSA) can now be performed using the new R package, QTLseqr. This tool aids in identifying quantitative trait loci (QTL) for genetic research.
Area of Science:
- Genetics
- Bioinformatics
- Computational Biology
Background:
- Next-Generation Sequencing Bulk Segregant Analysis (NGS-BSA) is a powerful technique for identifying quantitative trait loci (QTL).
- The R statistical platform is widely used in genetic research, but lacks a dedicated package for NGS-BSA.
- Existing methods for QTL detection can be computationally intensive or lack specific statistical rigor.
Purpose of the Study:
- To introduce QTLseqr, a novel R package designed to facilitate NGS-BSA.
- To provide two robust statistical approaches, QTL-seq and G', for QTL identification and significance assessment within the R environment.
- To offer a user-friendly tool for importing, filtering, and analyzing SNP data for QTL mapping.
Main Methods:
- Development of the QTLseqr R package, integrating simulation-based (QTL-seq) and statistic-based (G') methods.
- Implementation of functions for SNP data import, quality filtering, and distribution analysis.
- Calculation of relative allele frequencies, G' statistics, and log (-values) for QTL detection and visualization.
Main Results:
- QTLseqr successfully implements two distinct statistical approaches for QTL detection in NGS-BSA data.
- The package provides comprehensive tools for data processing, including SNP filtering and frequency calculations.
- QTLseqr enables the identification and plotting of significant quantitative trait loci, streamlining genetic analysis.
Conclusions:
- QTLseqr addresses the need for a dedicated R package for NGS-BSA, enhancing accessibility and efficiency.
- The package offers reliable methods for QTL identification and statistical validation.
- QTLseqr is a valuable resource for researchers aiming to map QTL using NGS-BSA data within the R statistical platform.
Related Concept Videos
Next-generation Sequencing
98.7K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
98.7K
DNA Packaging
112.8K
Overview
112.8K
Chromatin Packaging
19.3K
Each human somatic cell contains 6 billion base pairs of DNA. Each base pair is 0.34 nm long, meaning each diploid cell contains a staggering 2 meters of DNA. This long DNA strand is packed inside a nucleus measuring only 10-20 microns in diameter with the help of specialized DNA-binding proteins called histones. Together they form a compact DNA-protein complex called chromatin. The chromatin is further compacted into higher-order structures. The highest level of compaction is achieved during...
19.3K
Chromatin Packaging
22.2K
Each human somatic cell contains 6 billion base-pairs of DNA. Each base-pair is 0.34 nm long, which means that each diploid cell contains a staggering 2 meters of DNA. How is such a long DNA strand packed inside a nucleus measuring only 10 - 20 microns in diameter?
The chromatin
In combination with specialized DNA binding protein called Histones, the DNA double helix forms a compact DNA: protein complex called chromatin. The chromatin itself is further compacted into higher-order...
The chromatin
In combination with specialized DNA binding protein called Histones, the DNA double helix forms a compact DNA: protein complex called chromatin. The chromatin itself is further compacted into higher-order...
22.2K
Chromatin Packaging
9.8K
9.8K
Law of Segregation
78.2K
When crossing pea plants, Mendel noticed that one of the parental traits would sometimes disappear in the first generation of offspring, called the F1 generation, and could reappear in the next generation (F2). He concluded that one of the traits must be dominant over the other, thereby causing masking of one trait in the F1 generation. When he crossed the F1 plants, he found that 75% of the offspring in the F2 generation had the dominant phenotype, while 25% had the recessive phenotype.
78.2K

