Related Experiment Video
Updated: Sep 2, 2025

08:57
Using Phylogenetic Analysis to Investigate Eukaryotic Gene Origin
Published on: August 14, 2018
16.0K
HAlign 3: Fast Multiple Alignment of Ultra-Large Numbers of Similar DNA/RNA Sequences
Furong Tang1,2, Jiannan Chao1,3, Yanming Wei4
1Yangtze Delta Region Institute (Quzhou), University of Electronic Science and Technology of China, Quzhou, China.
Molecular Biology and Evolution
|August 1, 2022
Summary
HAlign 3 offers improved time efficiency and alignment quality for processing large DNA/RNA sequence datasets. This cross-platform tool is specialized for similar viral and prokaryotic genomes.
Area of Science:
- Bioinformatics
- Computational Biology
- Genomics
Background:
- Multiple sequence alignment (MSA) is crucial for understanding genomic relationships.
- Existing MSA tools face challenges with ultra-large datasets, particularly similar genomes.
- The center star strategy offers a framework for efficient MSA.
Purpose of the Study:
- To present significant updates to the HAlign program, version 3.
- To enhance the time efficiency and alignment quality of HAlign 3.
- To position HAlign 3 as a specialized tool for processing ultra-large, similar DNA/RNA sequence datasets.
Main Methods:
- HAlign 3 utilizes an updated center star strategy for multiple sequence alignment.
- The program is designed for high-throughput processing of genomic data.
- Cross-platform compatibility was ensured for macOS, Linux, and Windows systems.
Main Results:
- HAlign 3 demonstrates improved time efficiency compared to previous versions.
- The updated algorithm leads to enhanced alignment quality.
- The program effectively processes large datasets of similar viral and prokaryotic genomes.
Conclusions:
- HAlign 3 provides a powerful and efficient solution for large-scale sequence alignment.
- The specialized nature of HAlign 3 makes it ideal for comparative genomics of closely related organisms.
- Easy installation and open-source availability facilitate widespread adoption in bioinformatics research.
Related Concept Videos
Modern Molecular Taxonomy
117
Advancements in molecular biology have revolutionized the identification and characterization of bacteria, with multiple methods leveraging DNA sequencing for enhanced precision. As sequencing technologies improve and costs decline, these approaches are increasingly used in clinical, environmental, and evolutionary studies.Multilocus Sequence Typing (MLST) examines several housekeeping genes, essential chromosomal genes encoding cellular functions, to distinguish strains. Approximately...
117
Next-generation Sequencing
92.4K
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....
92.4K
Evolutionary Relationships through Genome Comparisons
6.1K
Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
6.1K
RNA-seq
10.3K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases.
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
10.3K

