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transAlign: using amino acids to facilitate the multiple alignment of protein-coding DNA sequences
1Lehrstuhl für Tierzucht, Technical University of Munich, Hochfeldweg 1, 85354 Freising-Weihenstephan, Germany. Olaf.Bininda@tierzucht.tum.de
BMC Bioinformatics
|June 23, 2005
Summary
This study introduces transAlign, a script for aligning protein-coding DNA sequences by translating them into amino acids. This method enhances alignment speed and accuracy, making it ideal for large-scale genomic analyses.
Area of Science:
- Genomics
- Bioinformatics
- Computational Biology
Background:
- Multiple sequence alignment is critical for comparative genomics and phylogenetic analysis.
- Aligning protein-coding DNA via amino acid sequences offers speed and accuracy advantages.
- Existing translated alignment tools are often incomplete, hindering large-scale automated applications.
Purpose of the Study:
- To develop a comprehensive and automated solution for aligning protein-coding DNA sequences using translated alignments.
- To improve the efficiency and accuracy of DNA sequence alignment for large datasets.
Main Methods:
- The transAlign script translates DNA sequences into amino acids.
- It utilizes ClustalW for amino acid sequence alignment.
- The aligned amino acid sequences are then back-translated to produce aligned DNA sequences, with options for handling frame shifts.
Main Results:
- transAlign provides a full, cross-platform implementation of translated alignments.
- The method demonstrably improves alignment speed and accuracy for protein-coding DNA sequences.
- Benchmarks show consistent performance gains across various datasets.
Conclusions:
- transAlign is highly suitable for large-scale, automated alignment of numerous protein-coding DNA datasets.
- The program offers user-definable options and robust performance.
- It is freely available as open-source software.