Abstract
Motivation: Recent advances in gene sequencing have provided complete sequence information for a number of genomes and as a result the amount of data in the sequence databases is growing at an exponential rate. We introduce here a new program, DbW, to automate the update of a functional family-specific multiple alignment that tries to include relevant sequences. The program is based on the use of different sources of information: sequences and annotations in databases. Results: The advantages of DbW are demonstrated using the 20 families of aminoacyl-tRNA synthetases, where DbW detects a maximum of homologous sequences in the Swiss-Prot and SPTREMBL databases. The global specificity of DbW in this test is 98.4% (1.6% of the sequences included in the alignment did not belong to the family according to their function), and the global sensitivity of DbW is estimated to be 95.2%. Thus, DbW provides a reliable basis for the many applications that rely on accurate multiple alignments, e.g. functional residue identification, 2D/3D structure prediction or homology modeling. © The Author 2004. Published by Oxford University Press. All rights reserved.
Cite
CITATION STYLE
Prigent, V., Thierry, J. C., Poch, O., & Plewniak, F. (2005). DbW: Automatic update of a functional family-specific multiple alignment. Bioinformatics, 21(8), 1437–1442. https://doi.org/10.1093/bioinformatics/bti218
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.