Fourier methods for biosequence analysis
- 1 January 1990
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 18 (21) , 6305-6310
- https://doi.org/10.1093/nar/18.21.6305
Abstract
Novel methods are discussed for using fast Fourier transforms for DNA or protein sequence comparison. These methods are also intended as a contribution to the more general computer science problem of text search. These methods extend the capabilities of previous FFT methods and show that these methods are capable of considerable refinement. In particular, novel methods are given which (1) enable the detection of clusters of matching letters, (2) facilitate the insertion of gaps to enhance sequence similarity, and (3) accommodate to varying densities of letters in the input sequence. These methods use Fourier analysis in two distinct ways. (1) Fast Fourier transforms are used to facilitate rapid computation. (2) Fourier expansions are used to form an ''image'' of the sequence comparision.This publication has 4 references indexed in Scilit:
- Methods for assessing the statistical significance of molecular sequence features by using general scoring schemes.Proceedings of the National Academy of Sciences, 1990
- Digital signal processing methods for biosequence comparisonNucleic Acids Research, 1990
- Improved tools for biological sequence comparison.Proceedings of the National Academy of Sciences, 1988
- An efficient method for matching nucleic acid sequencesNucleic Acids Research, 1982