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date | Mon, 23 May 2016 17:49:17 -0400 |
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/* Copyright 2009, 2010, 2012 Stéphane De Mita, Mathieu Siol This file is part of the EggLib library. EggLib is free software: you can redistribute it and/or modify it under the terms of the GNU General Public License as published by the Free Software Foundation, either version 3 of the License, or (at your option) any later version. EggLib is distributed in the hope that it will be useful, but WITHOUT ANY WARRANTY; without even the implied warranty of MERCHANTABILITY or FITNESS FOR A PARTICULAR PURPOSE. See the GNU General Public License for more details. You should have received a copy of the GNU General Public License along with EggLib. If not, see <http://www.gnu.org/licenses/>. */ #ifndef EGGLIB_MUTATOR_HPP #define EGGLIB_MUTATOR_HPP #include "DataMatrix.hpp" #include "Random.hpp" #include "Arg.hpp" #include "Mutation.hpp" namespace egglib { /** \brief Implements mutation models * * \ingroup coalesce * * Works with a previously built Ancestral Reconbination Graph. The * user must sets options using the setter-based interface. After * that he or she can call the method mute() that will generates * a DataMatrix object. * * Genotype data are represented by integer numbers. Regardless of * the mutation model, the ancestral state is always 0. The user can * set the rate of mutation (or, alternatively, fix the number of * mutations that occurred - which is the number of segregating sites * only with an infinite site model). * * Other options fall into two separate groups: the positions of the * mutated sites and the process of mutation (how new alleles are * generated). * * Concerning allele generation, several mutation models are available * (coded by single letters): * - F: fixed number of alleles. Among other markers, this model is * appropriate for simulating nucleotides. The user is able * to choose the number of alleles (where 2 is the standard * for an infinite site model and 4 for a finite site model). * Mutator allows assigning independent weights between all * different transition types and can draw randomly the * ancestral states, providing a way to emulate evolution of * nucleotides with multiple mutations at the same site and * reversion. * - I: infinite number of alleles. At a given site, each mutation * raises a new allele. The value of the alleles is therefore * irrelevant (it only denotes its order of appearance). This * model does not permit homoplasy. * - S: stepwise mutation model. In this model the value of the * alleles are interpreted as a size (typically for simulating * a microsatellite marker). Each mutation either increases * or decreases the allele size by an increment of one. * - T: two-phase mutation model. This model is a generalization * of the stepwise mutation model (S). For a mutation, the * increment (either increase or decrease) is 1 with the * probability given by the parameter (1-TPMproba). With * probability TPMproba, the increment is drawn from a * geometric distribution of parameter given by the other * parameter (TPMparam). * * By default, the program will assume an infinite site model (ISM). * Each mutation will occur to a new position drawn from the interval * [0,1]. It is possible to set any mutation model with an ISM * (including microsatellite-like models I, S and T). Alternatively, * the user can specify a finite number of sites available for * mutation. For a microsatellite marker, the user will want to * specify a single site. It is possible to set a finite number of * sites for all mutation models. In all cases, the mutations will * be forced to target these sites. It is possible to apply weights * independently to all sites. The higher the weight value * (comparatively to the other sites), the higher the probability * that this site mutes. The weights needs not to be relative. In * addition, the user can set the positions of the different sites. * Nothings forces him or her to place them in order. Note that this * does not affect the mutation process, but on the amount of * recombination that will be allowed between sites. * */ class Mutator { public: /** \brief Initializes with default values * * List of default values: * - theta = 0 * - fixedNumberOfMutations = 0 * - model = F (fixed number of alleles) * - fixed number of alleles = 2 * - infinite site model * - TPM parameters are both preset to 0.5 * */ Mutator(); /** \brief Destroys the object * */ ~Mutator(); /** \brief Copy constructor * */ Mutator(const Mutator&); /** \brief Assignement operator * */ Mutator& operator=(const Mutator&); /** \brief Restores default values of all parameters * */ void reset(); /** \brief Gets the fixed number of mutations * */ unsigned int fixedNumberOfMutations() const; /** \brief Sets the fixed number of mutations * * The value can be 0. It is not allowed to set both the * fixed number of mutations and the mutation rate at * non-zero value * */ void fixedNumberOfMutations(unsigned int); /** \brief Gets the mutation rate * */ double mutationRate() const; /** \brief Sets the mutation rate * * The value cannot be negative. The value can be 0. It is * not allowed to set both the fixed number of mutations and * the mutation rate at non-zero value * */ void mutationRate(double); /** \brief Gets the mutation model * * See the class documentation for the signification of the * different one-letter codes. * */ char mutationModel() const; /** \brief Sets the mutation model * * The passed character must be one of F, I, S and T. See the * class documentation for their signification. * */ void mutationModel(char); /** \brief Gets the fixed number of possible alleles * */ unsigned int numberOfAlleles() const; /** \brief Sets the fixed number of possible alleles * * The value must be larger than 1. This parameter is * meaningful only for the fixed number allele model of * mutation, and ignored otherwise. * */ void numberOfAlleles(unsigned int); /** \brief Sets a transition weight * * \param i row (previous allele index). * \param j column (next allele index). * \param value weight to apply. * * Indices i and j must be different. Weights can be any * strictly positive value. * */ void transitionWeight(unsigned int i, unsigned int j, double value); /** \brief Gets a transition weight * * \param i row (previous allele index). * \param j column (next allele index). * * Indices i and j must be different. * */ double transitionWeight(unsigned int i, unsigned int j); /** \brief Set to true to draw ancestral alleles randomly * * By default, the ancestral allele is always 0. If this * variable is set to true, the ancestral allele will be * randomly drawn from the defined number of alleles. This * option is always ignored unless in combination with the * Fixed Allele Number model. * */ void randomAncestralAllele(bool flag); /** \brief true if ancestral alleles must be drawn randomly * */ bool randomAncestralAllele() const; /** \brief Gets the TPM probability parameter * */ double TPMproba() const; /** \brief Sets the TPM probability parameter * * This parameter is considered only if the mutation model * is T (two-phase mutation model). It gives the probability * that a mutation step is not fixed to be 1. If TPMproba is * 0, the mutation model is SMM. * * The value must be >=0. and <=1. * */ void TPMproba(double value); /** \brief Gets the TPM distribution parameter * */ double TPMparam() const; /** \brief Sets the TPM distribution parameter * * This parameter is considered only if the mutation model * is T (two-phase mutation model). It gives the parameter * of the geometric distribution which is used to generate * the mutation step (if it is not one). * * The value must be >=0. and <=1. * */ void TPMparam(double value); /** \brief Gets the number of mutable sites * * A value a zero must be interpreted as the infinite site * model. Note that after all calls all data from the tables * sitePositions and siteWeights will be reset. * */ unsigned int numberOfSites() const; /** \brief Sets the number of mutable sites * * The value of zero is accepted and imposed the infinite * site model. * */ void numberOfSites(unsigned int); /** \brief Gets the position of a given site * */ double sitePosition(unsigned int siteIndex) const; /** \brief Set the position of a given site * * The position must be >=0 and <=1 * */ void sitePosition(unsigned int siteIndex, double position); /** \brief Gets the mutation weight of a given site * */ double siteWeight(unsigned int siteIndex) const; /** \brief Set the site weight of a given site * * The weight must be strictly positive. * */ void siteWeight(unsigned int siteIndex, double weight); /** \brief Performs mutation * * \param arg Ancestral recombination graph instance. If the * ARG is partially built or not a all, or improperly so, * the behaviour of this method is not defined. * * \param random The address of a Random instance to be * used for generating random numbers. * * \return A DataMatrix instance containing simulated data. * */ DataMatrix mute(Arg* arg, Random* random); /** \brief Gets the last number of mutations * * Returns the number of mutations of the last call of mute( ). * By default, this method returns 0. * */ unsigned int numberOfMutations() const; private: void clear(); void init(); void copy(const Mutator&); //int nextAllele(int allele, Random* random); int TPMstep(double inTPMproba, Random* random); void apply_mutation(unsigned int matrixIndex, unsigned int actualSite, DataMatrix& data, const Edge* edge, int allele, unsigned int segment, Random* random); char _model; double _mutationRate; unsigned int _fixedNumberOfMutations; unsigned int _numberOfAlleles; double** _transitionWeights; bool _randomAncestralAllele; unsigned int _numberOfSites; double* _sitePositions; double* _siteWeights; double _TPMproba; double _TPMparam; int maxAllele; unsigned int _numberOfMutations; std::vector<Mutation> _cache_mutations; unsigned int _cache_mutations_reserved; }; bool compare(Mutation mutation1, Mutation mutation2); // returns True if mutation1 is older } #endif