A general method for fast multiple sequence alignment

Tönges U, Perrey SW, Stoye J, Dress A (1996)
Gene 172(1): GC33-GC41.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
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Tönges, Udo; Perrey, Sören W.; Stoye, JensUniBi ; Dress, AndreasUniBi
Abstract / Bemerkung
We have developed a fast heuristic algorithm for multiple sequence alignment which provides near-to-optimal results for sufficiently homologous sequences. The algorithm makes use of the standard dynamic programming procedure by applying it to all pairs of sequences. The resulting score matrices for pair-wise alignment give rise to secondary matrices containing the additional charges imposed by forcing the alignment path to run through a particular vertex. Such a constraint corresponds to slicing the sequences at the positions defining that vertex, and aligning the remaining pairs of prefix and suffix sequences separately. From these secondary matrices, one can compute - for any given family of sequences - suitable positions for cutting all of these sequences simultaneously, thus reducing the problem of aligning a family of n sequences of average length l in a Divide and Conquer fashion to aligning two families of n sequences of approximately half that length. In this paper, we explain the method for the case of 3 sequences in detail, and we demonstrate its potential and its limits by discussing its behaviour for several test families. A generalization for aligning more than 3 sequences is lined out, and some actual alignments constructed by our algorithm for various user-defined parameters are presented.
Secondary matrix; Pair-wise sequence alignment; Divide and conquer; Multiple sequence alignment; Dynamic programming
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Tönges U, Perrey SW, Stoye J, Dress A. A general method for fast multiple sequence alignment. Gene. 1996;172(1):GC33-GC41.
Tönges, U., Perrey, S. W., Stoye, J., & Dress, A. (1996). A general method for fast multiple sequence alignment. Gene, 172(1), GC33-GC41. https://doi.org/10.1016/0378-1119(96)00123-0
Tönges, Udo, Perrey, Sören W., Stoye, Jens, and Dress, Andreas. 1996. “A general method for fast multiple sequence alignment”. Gene 172 (1): GC33-GC41.
Tönges, U., Perrey, S. W., Stoye, J., and Dress, A. (1996). A general method for fast multiple sequence alignment. Gene 172, GC33-GC41.
Tönges, U., et al., 1996. A general method for fast multiple sequence alignment. Gene, 172(1), p GC33-GC41.
U. Tönges, et al., “A general method for fast multiple sequence alignment”, Gene, vol. 172, 1996, pp. GC33-GC41.
Tönges, U., Perrey, S.W., Stoye, J., Dress, A.: A general method for fast multiple sequence alignment. Gene. 172, GC33-GC41 (1996).
Tönges, Udo, Perrey, Sören W., Stoye, Jens, and Dress, Andreas. “A general method for fast multiple sequence alignment”. Gene 172.1 (1996): GC33-GC41.

11 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

The relative sensitivity of different alignment methods and character codings in sensitivity analysis
Simmons MarkP, Müller KaiF, Webb ColleenT., Cladistics 24(6), 2008
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Sammeth M, Heringa J., Proteins 64(1), 2006
PMID: 16609972
Detailed protein sequence alignment based on Spectral Similarity Score (SSS).
Gupta K, Thomas D, Vidya SV, Venkatesh KV, Ramakumar S., BMC Bioinformatics 6(), 2005
PMID: 15850477

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