Optimal alignment between groups of sequences and its application to multiple sequence alignment
By O. Gotoh. 1993
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
- Robert C. Edgar
- Kazutaka Katoh
- Lior S. Pachter
- Nick V. Grishin
- Ruslan I. Sadreyev
- Anna R. Panchenko
- Kazunori D. Yamada
- K. Kuma
Citations in the corpus
- MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability (2013, methodology): “As listed in table 1, MAFFT version 7 has options for various alignment strategies, including progressive methods (PartTree, FFT-NS-1, and L-INS-1) (Feng and Doolittle 1987; Higgins and Sharp 1988; Katoh and Toh 2007), iterative refinement methods (FFT-NS-i, L-INS-i, E-INS-i, and G-INS-i) (Barton and”
- Finding weak similarities between proteins by sequence profile comparison. (2003, methodology): “For example, in the progressive and iterative multiple alignment methods two groups of sequences have been compared using the weighted ‘sum of pairs’ score ( 12 ,13).”
- Application of the MAFFT sequence alignment program to large data—reexamination of the usefulness of chained guide trees (2016, methodology): “It is known that the iterative refinement technique (Barton and Sternberg, 1987; Berger and Munson, 1991; Gotoh, 1993) improves the accuracy of an MSA in comparison with the progressive method.”
- Metrics and Similarity Measures for Hidden Markov Models (1999, background): “These models do not strictly follow the profile architecture and consequently cannot be compared using profile ’align-ment (Gotoh 1993).”
- Recent developments in the MAFFT multiple sequence alignment program (2008, methodology): “Various combinations of objective functions and optimization strategies have been proposed to date [55–61].”
- COMPASS: a tool for comparison of multiple protein alignments with assessment of statistical significance. (2003, methodology): “BLOSUM62). lu derived from equation ( 12 ) depends only on the residue composition of the profiles or sequences.”
- MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform. (2002, methodology): “To overcome this difficulty, various heuristic methods, including progressive methods (3) and iterative refinement methods (4–6), have been proposed to date.”
- Multiple sequence alignment using partial order graphs (2002, background): “…different advantages and disadvantages (Taylor, 1986; Barton and Sternberg, 1987; Altschul, 1989; Lipman et al., 1989; Subbiah and Harrison, 1989; Gotoh, 1993, 1996; Thompson et al., 1994; Notredame et al., 2000; Gordon et al., 2001), but globally optimal alignment of larger numbers of sequences…”
- OXBench: A benchmark for evaluation of protein multiple sequence alignment accuracy (2003, unknown): “Gotoh [17] assessed the multiple sequence alignment method CLUSTALW [8]; and four of his own methods [18–20], on 54 families from the Joy 3.2 database [21] of alignments from 3D structure comparisons.”
- MAVID: constrained ancestral alignment of multiple sequences. (2003, methodology): “Iterative refinement, the process of re-aligning across an edge in the tree, fits in naturally with our framework [Gotoh 1993, Gotoh 1996].”