Results 1  10
of
58
Fast Folding and Comparison of RNA Secondary Structures (The Vienna RNA Package)
"... Computer codes for computation and comparison of RNA secondary structures, the Vienna RNA package, are presented, that are based on dynamic programming algorithms and aim at predictions of structures with minimum free energies as well as at computations of the equilibrium partition functions and bas ..."
Abstract

Cited by 473 (90 self)
 Add to MetaCart
Computer codes for computation and comparison of RNA secondary structures, the Vienna RNA package, are presented, that are based on dynamic programming algorithms and aim at predictions of structures with minimum free energies as well as at computations of the equilibrium partition functions and base pairing probabilities. An efficient heuristic for the inverse folding problem of RNA is introduced. In addition we present compact and efficient programs for the comparison of RNA secondary structures based on tree editing and alignment. All computer codes are written in ANSI C. They include implementations of modified algorithms on parallel computers with distributed memory. Performance analysis carried out on an Intel Hypercube shows that parallel computing becomes gradually more and more efficient the longer the sequences are.
The Schema Theorem and Price's Theorem
 FOUNDATIONS OF GENETIC ALGORITHMS
, 1995
"... Holland's Schema Theorem is widely taken to be the foundation for explanations of the power of genetic algorithms (GAs). Yet some dissent has been expressed as to its implications. Here, dissenting arguments are reviewed and elaborated upon, explaining why the Schema Theorem has no implications f ..."
Abstract

Cited by 93 (3 self)
 Add to MetaCart
Holland's Schema Theorem is widely taken to be the foundation for explanations of the power of genetic algorithms (GAs). Yet some dissent has been expressed as to its implications. Here, dissenting arguments are reviewed and elaborated upon, explaining why the Schema Theorem has no implications for how well a GA is performing. Interpretations of the Schema Theorem have implicitly assumed that a correlation exists between parent and offspring fitnesses, and this assumption is made explicit in results based on Price's Covariance and Selection Theorem. Schemata do not play a part in the performance theorems derived for representations and operators in general. However, schemata reemerge when recombination operators are used. Using Geiringer's recombination distribution representation of recombination operators, a "missing" schema theorem is derived which makes explicit the intuition for when a GA should perform well. Finally, the method of "adaptive landscape" analysis is exa...
Landscapes and Their Correlation Functions
, 1996
"... Fitness landscapes are an important concept in molecular evolution. Many important examples of landscapes in physics and combinatorial optimation, which are widely used as model landscapes in simulations of molecular evolution and adaptation, are "elementary", i.e., they are (up to an additive const ..."
Abstract

Cited by 89 (15 self)
 Add to MetaCart
Fitness landscapes are an important concept in molecular evolution. Many important examples of landscapes in physics and combinatorial optimation, which are widely used as model landscapes in simulations of molecular evolution and adaptation, are "elementary", i.e., they are (up to an additive constant) eigenfuctions of a graph Laplacian. It is shown that elementary landscapes are characterized by their correlation functions. The correlation functions are in turn uniquely determined by the geometry of the underlying configuration space and the nearest neighbor correlation of the elementary landscape. Two types of correlation functions are investigated here: the correlation of a time series sampled along a random walk on the landscape and the correlation function with respect to a partition of the set of all vertex pairs.
Generic Properties of Combinatory Maps  Neutral Networks of RNA Secondary Structures
, 1995
"... Random graph theory is used to model relationships between sequences and secondary structures of RNA molecules. Sequences folding into identical structures form neutral networks which percolate sequence space if the fraction of neutral nearest neighbors exceeds a threshold value. The networks of any ..."
Abstract

Cited by 80 (36 self)
 Add to MetaCart
Random graph theory is used to model relationships between sequences and secondary structures of RNA molecules. Sequences folding into identical structures form neutral networks which percolate sequence space if the fraction of neutral nearest neighbors exceeds a threshold value. The networks of any two different structures almost touch each other, and sequences folding into almost all "common" structures can be found in a small ball of an arbitrary location in sequence space. The results from random graph theory are compared with data obtained by folding large samples of RNA sequences. Differences are explained in terms of RNA molecular structures. 1.
Analysis of RNA Sequence Structure Maps by Exhaustive Enumeration
, 1996
"... Global relations between RNA sequences and secondary structues are understood as mappings from sequence space into shape space. These mappings are investigated by exhaustive folding of all GC and AU sequences with chain lengths up to 30. The technique od tries is used for economic data storage and f ..."
Abstract

Cited by 73 (35 self)
 Add to MetaCart
Global relations between RNA sequences and secondary structues are understood as mappings from sequence space into shape space. These mappings are investigated by exhaustive folding of all GC and AU sequences with chain lengths up to 30. The technique od tries is used for economic data storage and fast retrieval of information. The computed structural data are evaluated through exhaustive enumeration and used as an exact reference for testing analytical results derived from mathematical models and sampling based of statistical methods. Several new concepts of RNA sequence to secondary structure mappings are investigated, among them the structure of neutral networks (being sets of sequences folding into the same structure), percolation of sequence space by neutral networks, and the principle of shape space covering . The data of exhaustive enumeration are compared to the analytical results of a random graph model that reveals the generic properties of sequence to structure mappings based on some base pairing logic. The differences between the numerical and the analytical results are interpreted in terms of specific biophysical properties of RNA molecules.
Fitness Landscapes
 Appl. Math. & Comput
, 2002
"... . Fitness landscapes are a valuable concept in evolutionary biology, combinatorial optimization, and the physics of disordered systems. A fitness landscape is a mapping from a configuration space that is equipped with some notion of adjacency, nearness, distance or accessibility, into the real numbe ..."
Abstract

Cited by 64 (14 self)
 Add to MetaCart
. Fitness landscapes are a valuable concept in evolutionary biology, combinatorial optimization, and the physics of disordered systems. A fitness landscape is a mapping from a configuration space that is equipped with some notion of adjacency, nearness, distance or accessibility, into the real numbers. Landscape theory has emerged as an attempt to devise suitable mathematical structures for describing the "static" properties of landscapes as well as their influence on the dynamics of adaptation. This chapter gives a brief overview on recent developments in this area, focusing on "geometrical" properties of landscapes. 1 Introduction The concept of a fitness landscape originated in theoretical biology more than seventy years ago [1]. It can be thought of as a kind of "potential function" underlying the dynamics of evolutionary optimization. Implicit in this idea is both a fitness function f that assigns a fitness value to every possible genotype (or organism), and the arrangement of t...
Ruggedness and Neutrality  The NKp family of Fitness Landscapes
 Alive VI: Sixth International Conference on Articial Life
, 1998
"... It has come to be almost an article of faith amongst population biologists and GA researchers alike that the principal feature of a fitness landscape as regards evolutionary dynamics is "ruggedness", particularly as measured by the autocorrelation function. In this paper we demonstrate that autoco ..."
Abstract

Cited by 45 (2 self)
 Add to MetaCart
It has come to be almost an article of faith amongst population biologists and GA researchers alike that the principal feature of a fitness landscape as regards evolutionary dynamics is "ruggedness", particularly as measured by the autocorrelation function. In this paper we demonstrate that autocorrelation alone may be inadequate as a mediator of evolutionary dynamics, specifically in the presence of large scale neutrality. We introduce the NKp family of landscapes (a variant on NK landscapes) which possess the remarkable property that varying the degree of neutrality has minimal effect on the correlation structure. It is demonstrated that NKp landscapes feature neutral networks which have a "constant innovation" property comparable with the neutral networks observed in models of RNA secondary structure folding landscapes. We show that evolutionary dynamics on NKp landscapes vary dramatically with the degree of neutrality  at high neutrality the dynamics are characterised by populat...
Landscapes  Complex Optimization Problems and Biopolymer Structures
 Computers Chem
, 1993
"... The evolution of RNA molecules in replication assays, viroids and RNA viruses can be viewed as an adaptation process on a 'fitness' landscape. The dynamics of evolution is hence tightly linked to the structure of the underlying landscape. Global features of landscapes can be described by statistical ..."
Abstract

Cited by 31 (16 self)
 Add to MetaCart
The evolution of RNA molecules in replication assays, viroids and RNA viruses can be viewed as an adaptation process on a 'fitness' landscape. The dynamics of evolution is hence tightly linked to the structure of the underlying landscape. Global features of landscapes can be described by statistical measures like number of optima, lengths of walks, and correlation functions. The evolution of a quasispecies on such landscapes exhibits three dynamical regimes depending on the replication fidelity: Above the "localization threshold" the population is centered around a (local) optimum. Between localization and "dispersion threshold" the population is still centered around a consensus sequence, which, however, changes in time. For very large mutation rates the population spreads in sequence space like a gas. The critical mutation rates separating the three domains depend strongly on characteristics properties of the fitness landscapes. Statistical characteristics of RNA landscapes are acces...
The algebraic theory of recombination spaces
, 2000
"... A new mathematical representation is proposed for the configuration space structure induced by recombination which we called "Pstructure". It consists of a mapping of pairs of objects to the power set of all objects in the search space. The mapping assigns to each pair of parental "genotypes" the s ..."
Abstract

Cited by 29 (15 self)
 Add to MetaCart
A new mathematical representation is proposed for the configuration space structure induced by recombination which we called "Pstructure". It consists of a mapping of pairs of objects to the power set of all objects in the search space. The mapping assigns to each pair of parental "genotypes" the set of all recombinant genotypes obtainable from the parental ones. It is shown that this construction allows a Fourierdecomposition of fitness landscapes into a superposition of "elementary landscapes". This decomposition is analogous to the Fourier decomposition of fitness landscapes on mutation spaces. The elementary landscapes are obtained as eigenfunctions of a Laplacian operator defined for Pstructures. For binary string recombination the elementary landscapes are exactly the pspin functions (Walsh functions), i.e. the same as the elementary landscapes of the string point mutation spaces (i.e. the hypercube). This supports the notion of a strong homomorphisms between string mutation ...
Evolutionary Dynamics and Optimization  Neutral Networks as ModelLandscapes for RNA SecondaryStructure FoldingLandscapes
, 1995
"... We view the folding of RNAsequences as a map that assigns a pattern of base pairings to each sequence, known as secondary structure. These preimages can be constructed as random graphs (i.e. the neutral networks associated to the structure s). By interpreting the secondary structure as biological i ..."
Abstract

Cited by 26 (6 self)
 Add to MetaCart
We view the folding of RNAsequences as a map that assigns a pattern of base pairings to each sequence, known as secondary structure. These preimages can be constructed as random graphs (i.e. the neutral networks associated to the structure s). By interpreting the secondary structure as biological information we can formulate the so called Error Threshold of Shapes as an extension of Eigen's et al. concept of an error threshold in the single peak landscape [5]. Analogue to the approach of Derrida & Peliti [3] for a flat landscape we investigate the spatial distribution of the population on the neutral network. On the one hand this model of a single shape landscape allows the derivation of analytical results, on the other hand the concept gives rise to study various scenarios by means of simulations, e.g. the interaction of two different networks [29]. It turns out that the intersection of two sets of compatible sequences (with respect to the pair of secondary structures) plays a key role in the search for "fitter" secondary structures.