Chain growth algorithms for HP-type lattice proteins
RECOMB '97 Proceedings of the first annual international conference on Computational molecular biology
On the complexity of protein folding (extended abstract)
STOC '98 Proceedings of the thirtieth annual ACM symposium on Theory of computing
Exploring high-dimensional energy landscapes
Computing in Science and Engineering
Distributed projects tackle protein mystery
Computing in Science and Engineering
Computational studies of protein folding
Computing in Science and Engineering
Introduction to Algorithms
A complete and effective move set for simplified protein folding
RECOMB '03 Proceedings of the seventh annual international conference on Research in computational molecular biology
Genetic Algorithm for 3D Protein Folding Simulations
Proceedings of the 5th International Conference on Genetic Algorithms
Practical Genetic Algorithms with CD-ROM
Practical Genetic Algorithms with CD-ROM
Blue Gene: a vision for protein science using a petaflop supercomputer
IBM Systems Journal - Deep computing for the life sciences
Generalized schemata theorem incorporating twin removal for protein structure prediction
PRIB'07 Proceedings of the 2nd IAPR international conference on Pattern recognition in bioinformatics
AI'06 Proceedings of the 19th Australian joint conference on Artificial Intelligence: advances in Artificial Intelligence
IEEE Transactions on Evolutionary Computation
An Immune Algorithm for Protein Structure Prediction on Lattice Models
IEEE Transactions on Evolutionary Computation
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Nondeterministic conformational search techniques, such as Genetic Algorithms (GAs) are promising for solving protein structure prediction (PSP) problem. The crossover operator of a GA can underpin the formation of potential conformations by exchanging and sharing potential sub-conformations, which is promising for solving PSP. However, the usual nature of an optimum PSP conformation being compact can produce many invalid conformations (by having non-self-avoiding-walk) using crossover. While a crossover-based converging conformation suffers from limited pathways, combining it with depth-first search (DFS) can partially reveal potential pathways. DFS generates random conformations increasingly quickly with increasing length of the protein sequences compared to random-move-only-based conformation generation. Random conformations are frequently applied for maintaining diversity as well as for initialization in many GA variations.