Abstract
Constructing multiple homologous alignments for protein-coding DNA sequences is crucial for a variety of bioinformatic analyses but remains computationally challenging. With the growing amount of sequence data available and the ongoing efforts largely dependent on protein-coding DNA alignments, there is an increasing demand for a tool that can process a large number of homologous groups and generate multiple protein-coding DNA alignments. Here we present a parallel tool - ParaAT that is capable of parallelly constructing multiple protein-coding DNA alignments for a large number of homologs. As testified on empirical datasets, ParaAT is well suited for large-scale data analysis in the high-throughput era, providing good scalability and exhibiting high parallel efficiency for computationally demanding tasks. ParaAT is freely available for academic use only at http://cbb.big.ac.cn/software.
Original language | English |
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Pages (from-to) | 779-781 |
Number of pages | 3 |
Journal | Biochemical and Biophysical Research Communications |
Volume | 419 |
Issue number | 4 |
DOIs | |
Publication status | Published - 23 Mar 2012 |
Keywords
- Alignment
- Back-translation
- Homolog
- Parallel
- Protein-coding DNA alignment