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Randomization.bib
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% Generated by Paperpile. Check out https://paperpile.com for more information.
% BibTeX export options can be customized via Settings -> BibTeX.
@ARTICLE{Beaumont2010-vr,
title = "Approximate Bayesian Computation in Evolution and Ecology",
author = "Beaumont, Mark A",
journal = "Annu. Rev. Ecol. Evol. Syst.",
volume = 41,
number = 1,
pages = "379--406",
year = 2010,
url = "http://www.annualreviews.org/doi/abs/10.1146/annurev-ecolsys-102209-144621",
keywords = "ABC;Module - Randomization",
issn = "1543-592X",
doi = "10.1146/annurev-ecolsys-102209-144621",
original_id = "855cf87d-7976-0e5e-a3fc-ef5e2f1b10c3"
}
@ARTICLE{Storey2003-mz,
title = "Statistical significance for genomewide studies",
author = "Storey, John D and Tibshirani, Robert",
abstract = "With the increase in genomewide experiments and the sequencing
of multiple genomes, the analysis of large data sets has
become commonplace in biology. It is often the case that
thousands of features in a genomewide data set are tested
against some null hypothesis, where a number of features are
expected to be significant. Here we propose an approach to
measuring statistical significance in these genomewide studies
based on the concept of the false discovery rate. This
approach offers a sensible balance between the number of true
and false positives that is automatically calibrated and
easily interpreted. In doing so, a measure of statistical
significance called the q value is associated with each tested
feature. The q value is similar to the well known p value,
except it is a measure of significance in terms of the false
discovery rate rather than the false positive rate. Our
approach avoids a flood of false positive results, while
offering a more liberal criterion than what has been used in
genome scans for linkage.",
journal = "Proc. Natl. Acad. Sci. U. S. A.",
volume = 100,
number = 16,
pages = "9440--9445",
month = aug,
year = 2003,
url = "http://dx.doi.org/10.1073/pnas.1530509100",
keywords = "xx Archived/FDR;Module - Randomization;Quantitative Methods",
language = "en",
issn = "0027-8424",
pmid = "12883005",
doi = "10.1073/pnas.1530509100",
pmc = "PMC170937",
original_id = "cb386ad5-cd57-0385-8c7c-4dbdf850cef6"
}
@ARTICLE{Benjamini1995-cw,
title = "Controlling the False Discovery Rate: A Practical and Powerful
Approach to Multiple Testing",
author = "Benjamini, Yoav and Hochberg, Yosef",
abstract = "The common approach to the multiplicity problem calls for
controlling the familywise error rate (FWER). This approach,
though, has faults, and we point out a few. A different
approach to problems of multiple significance testing is
presented. It calls for controlling the expected proportion of
falsely rejected hypotheses-the false discovery rate. This
error rate is equivalent to the FWER when all hypotheses are
true but is smaller otherwise. Therefore, in problems where
the control of the false discovery rate rather than that of
the FWER is desired, there is potential for a gain in power. A
simple sequential Bonferroni-type procedure is proved to
control the false discovery rate for independent test
statistics, and a simulation study shows that the gain in
power is substantial. The use of the new procedure and the
appropriateness of the criterion are illustrated with
examples.",
journal = "J. R. Stat. Soc. Series B Stat. Methodol.",
volume = 57,
number = 1,
pages = "289--300",
year = 1995,
url = "http://www.jstor.org/stable/2346101",
keywords = "xx Archived/FDR;Module - Randomization;Quantitative Methods",
issn = "1369-7412, 0035-9246",
original_id = "f82b0881-aae3-0dd0-9d8d-150bd55279dc"
}
@ARTICLE{Curran-Everett2000-qv,
title = "Multiple comparisons: philosophies and illustrations",
author = "Curran-Everett, Douglas",
abstract = "Statistical procedures underpin the process of scientific
discovery. As researchers, one way we use these procedures is
to test the validity of a null hypothesis. Often, we test the
validity of more than one null hypothesis. If we fail to use
an appropriate procedure to account for this multiplicity,
then we are more likely to reach a wrong scientific
conclusion[---]we are more likely to make a mistake. In
physiology, experiments that involve multiple comparisons are
common: of the original articles published in 1997 by the
American Physiological Society, ~40\% cite a multiple
comparison procedure. In this review, I demonstrate the
statistical issue embedded in multiple comparisons, and I
summarize the philosophies of handling this issue. I also
illustrate the three procedures[---]Newman-Keuls, Bonferroni,
least significant difference[---]cited most often in my
literature review; each of these procedures is of limited
practical value. Last, I demonstrate the false discovery rate
procedure, a promising development in multiple comparisons.
The false discovery rate procedure may be the best practical
solution to the problems of multiple comparisons that exist
within physiology and other scientific disciplines.",
journal = "Am. J. Physiol. Regul. Integr. Comp. Physiol.",
volume = 279,
number = 1,
pages = "R1--8",
month = jul,
year = 2000,
url = "http://ajpregu.physiology.org/content/279/1/R1",
keywords = "xx Archived/FDR;Module - Randomization;Quantitative Methods",
issn = "0363-6119",
original_id = "42551e24-cdd3-0e20-8f12-bfcc634958d6"
}
@ARTICLE{Blum2010-ol,
title = "Non-linear regression models for Approximate Bayesian
Computation",
author = "Blum, Michael G B and François, Olivier",
abstract = "Approximate Bayesian inference on the basis of summary
statistics is well-suited to complex problems for which the
likelihood is either mathematically or computationally
intractable. However the methods that use rejection suffer
from the curse of dimensionality when the number of summary
statistics is increased. Here we propose a machine-learning
approach to the estimation of the posterior density by
introducing two innovations. The new method fits a nonlinear
conditional heteroscedastic regression of the parameter on the
summary statistics, and then adaptively improves estimation
using importance sampling. The new algorithm is compared to
the state-of-the-art approximate Bayesian methods, and
achieves considerable reduction of the computational burden in
two examples of inference in statistical genetics and in a
queueing model.",
journal = "Stat. Comput.",
publisher = "Springer US",
volume = 20,
number = 1,
pages = "63--73",
month = jan,
year = 2010,
url = "http://link.springer.com/article/10.1007/s11222-009-9116-0",
keywords = "ABC;Module - Randomization;Bayes Readings;Module - Bayes",
language = "en",
issn = "0960-3174, 1573-1375",
doi = "10.1007/s11222-009-9116-0",
original_id = "3154d38c-98ee-09d6-b910-2d5db2013a92"
}
@MISC{Amabile1989-pf,
title = "Against all odds inside statistics",
author = "Amabile, Teresa",
publisher = "Annenberg/CPB Collection; Intellimation [distributor]",
year = 1989,
keywords = "Module - Randomization;Quantitative Methods",
original_id = "d6afabeb-5756-0421-94a3-407472185c27"
}
@ARTICLE{Brauer2002-ks,
title = "Genetic algorithms and parallel processing in
maximum-likelihood phylogeny inference",
author = "Brauer, M and Holder, Mark and Dries, L and Zwickl, Derrick
and Lewis, Paul O and Hillis, David M",
abstract = "We investigated the usefulness of a parallel genetic algorithm
for phylogenetic inference under the maximum-likelihood (NIL)
optimality criterion. Parallelization was accomplished by
assigning each ``individual'' in the genetic algorithm
``population'' to a separate processor so that the number of
processors used was equal to the size of the evolving
population (plus one additional processor for the control of
operations). The genetic algorithm incorporated branch-length
and topological mutation, recombination, selection on the ML
score, and (in some cases) migration and recombination among
subpopulations. We tested this parallel genetic algorithm with
large (228 taxa) data sets of both empirically observed DNA
sequence data (for angiosperms) as well as simulated DNA
sequence data. For both observed and simulated data,
search-time improvement was nearly linear with respect to the
number of processors, so the parallelization strategy appears
to be highly effective at improving computation time for large
phylogenetic problems using the genetic algorithm. We also
explored various ways of optimizing and tuning the parameters
of the genetic algorithm. Under the conditions of our
analyses, we did not find the best-known solution using the
genetic algorithm approach before terminating each run. We
discuss some possible limitations of the current
implementation of this genetic algorithm as well as of avenues
for its future improvement.",
journal = "Mol. Biol. Evol.",
volume = 19,
number = 10,
pages = "1717--1726",
year = 2002,
keywords = "Genetic algorithm;Module - Randomization",
issn = "0737-4038",
original_id = "e8a5f52b-c7cf-0d21-be86-98ed49f2a111"
}
@ARTICLE{Zwickl2008-yy,
title = "{GARLI}: Genetic Algorithm for Rapid Likelihood Inference",
author = "Zwickl, Derrick",
journal = "Presentations",
pages = "87",
year = 2008,
keywords = "Genetic algorithm;Module - Randomization",
issn = "1041-9780",
original_id = "713926f5-5cac-0978-82f5-2d0699cf0931"
}
@ARTICLE{Csillery2010-dj,
title = "Approximate Bayesian Computation ({ABC}) in practice",
author = "Csilléry, Katalin and Blum, Michael G B and Gaggiotti, Oscar E
and François, Olivier",
journal = "Trends Ecol. Evol.",
volume = 25,
number = 7,
pages = "410--418",
year = 2010,
url = "http://dx.doi.org/10.1016/j.tree.2010.04.001",
keywords = "ABC;Module - Randomization",
issn = "0169-5347",
pmid = "20488578",
doi = "10.1016/j.tree.2010.04.001",
original_id = "f0698de0-8c5c-03c0-a792-d8fcdd808a2f"
}
@ARTICLE{Beaumont2002-kn,
title = "Approximate Bayesian Computation in Population Genetics",
author = "Beaumont, Mark A and Zhang, Wenyang and Balding, David J",
abstract = "We propose a new method for approximate Bayesian statistical
inference on the basis of summary statistics. The method is
suited to complex problems that arise in population genetics,
extending ideas developed in this setting by earlier authors.
Properties of the posterior distribution of a parameter, such
as its mean or density curve, are approximated without
explicit likelihood calculations. This is achieved by fitting
a local-linear regression of simulated parameter values on
simulated summary statistics, and then substituting the
observed summary statistics into the regression equation. The
method combines many of the advantages of Bayesian statistical
inference with the computational efficiency of methods based
on summary statistics. A key advantage of the method is that
the nuisance parameters are automatically integrated out in
the simulation step, so that the large numbers of nuisance
parameters that arise in population genetics problems can be
handled without difficulty. Simulation results indicate
computational and statistical efficiency that compares
favorably with those of alternative methods previously
proposed in the literature. We also compare the relative
efficiency of inferences obtained using methods based on
summary statistics with those obtained directly from the data
using MCMC.",
journal = "Genetics",
volume = 162,
number = 4,
pages = "2025--2035",
month = dec,
year = 2002,
url = "http://www.genetics.org/content/162/4/2025",
keywords = "ABC;Module - Randomization",
language = "en",
issn = "0016-6731, 1943-2631",
pmid = "12524368",
original_id = "76290b01-59ff-0930-8ea5-fb8d032ed3ec"
}
@ARTICLE{Scrucca2013-jf,
title = "{GA}: A Package for Genetic Algorithms in {R}",
author = "Scrucca, Luca",
abstract = "Genetic algorithms (GAs) are stochastic search algorithms
inspired by the basic principles of biological evolution and
natural selection. GAs simulate the evolution of living
organisms, where the fittest individuals dominate over the weaker
ones, by mimicking the biological mechanisms of evolution, such
as selection, crossover and mutation. GAs have been successfully
applied to solve optimization problems, both for continuous
(whether differentiable or not) and discrete functions. This
paper describes the R package GA, a collection of general purpose
functions that provide a flexible set of tools for applying a
wide range of genetic algorithm methods. Several examples are
discussed, ranging from mathematical functions in one and two
dimensions known to be hard to optimize with standard
derivative-based methods, to some selected statistical problems
which require the optimization of user defined objective
functions. (This paper contains animations that can be viewed
using the Adobe Acrobat PDF viewer.)",
journal = "Journal of Statistical Software",
volume = 53,
number = 4,
pages = "1--37",
year = 2013,
url = "https://www.jstatsoft.org/v053/i04",
keywords = "Genetic algorithm;Module - Randomization",
issn = "1548-7660",
doi = "10.18637/jss.v053.i04"
}
@ARTICLE{Mebane2011-vy,
title = "Genetic optimization using derivatives: The rgenoud package for
{R}",
author = "Mebane, Jr, Walter and Sekhon, Jasjeet",
abstract = "genoud is an R function that combines evolutionary algorithm
methods with a derivative-based (quasi-Newton) method to solve
difficult optimization problems. genoud may also be used for
optimization problems for which derivatives do not exist. genoud
solves problems that are nonlinear or perhaps even discontinuous
in the parameters of the function to be optimized. When the
function to be optimized (for example, a log-likelihood) is
nonlinear in the model's parameters, the function will generally
not be globally concave and may have irregularities such as
saddlepoints or discontinuities. Optimization methods that rely
on derivatives of the objective function may be unable to find
any optimum at all. Multiple local optima may exist, so that
there is no guarantee that a derivative-based method will
converge to the global optimum. On the other hand, algorithms
that do not use derivative information (such as pure genetic
algorithms) are for many problems needlessly poor at local hill
climbing. Most statistical problems are regular in a neighborhood
of the solution. Therefore, for some portion of the search space,
derivative information is useful. The function supports parallel
processing on multiple CPUs on a single machine or a cluster of
computers.",
journal = "Journal of Statistical Software",
volume = 42,
number = 11,
pages = "1--26",
year = 2011,
url = "https://www.jstatsoft.org/v042/i11",
keywords = "Genetic algorithm;Module - Randomization",
issn = "1548-7660",
doi = "10.18637/jss.v042.i11"
}
@ARTICLE{Turner2012-rw,
title = "A tutorial on approximate Bayesian computation",
author = "Turner, Brandon M and Van Zandt, Trisha",
abstract = "This tutorial explains the foundation of approximate Bayesian
computation (ABC), an approach to Bayesian inference that does
not require the specification of a likelihood function, and hence
that can be used to estimate posterior distributions of
parameters for simulation-based models. We discuss briefly the
philosophy of Bayesian inference and then present several
algorithms for ABC. We then apply these algorithms in a number of
examples. For most of these examples, the posterior distributions
are known, and so we can compare the estimated posteriors derived
from ABC to the true posteriors and verify that the algorithms
recover the true posteriors accurately. We also consider a
popular simulation-based model of recognition memory (REM) for
which the true posteriors are unknown. We conclude with a number
of recommendations for applying ABC methods to solve real-world
problems.",
journal = "J. Math. Psychol.",
volume = 56,
number = 2,
pages = "69--85",
month = apr,
year = 2012,
url = "http://www.sciencedirect.com/science/article/pii/S0022249612000272",
keywords = "Approximate Bayesian computation; Tutorial; Bayesian estimation;
Population Monte Carlo;ABC;Module - Randomization;Bayes
Readings;Module - Bayes",
issn = "0022-2496",
doi = "10.1016/j.jmp.2012.02.005"
}
@ARTICLE{Pritchard1999-uh,
title = "Population growth of human {Y} chromosomes: a study of {Y}
chromosome microsatellites",
author = "Pritchard, J K and Seielstad, M T and Perez-Lezaun, A and
Feldman, M W",
abstract = "We use variation at a set of eight human Y chromosome
microsatellite loci to investigate the demographic history of the
Y chromosome. Instead of assuming a population of constant size,
as in most of the previous work on the Y chromosome, we consider
a model which permits a period of recent population growth. We
show that for most of the populations in our sample this model
fits the data far better than a model with no growth. We estimate
the demographic parameters of this model for each population and
also the time to the most recent common ancestor. Since there is
some uncertainty about the details of the microsatellite mutation
process, we consider several plausible mutation schemes and
estimate the variance in mutation size simultaneously with the
demographic parameters of interest. Our finding of a recent
common ancestor (probably in the last 120,000 years), coupled
with a strong signal of demographic expansion in all populations,
suggests either a recent human expansion from a small ancestral
population, or natural selection acting on the Y chromosome.",
journal = "Mol. Biol. Evol.",
volume = 16,
number = 12,
pages = "1791--1798",
month = dec,
year = 1999,
url = "http://dx.doi.org/10.1093/oxfordjournals.molbev.a026091",
keywords = "ABC;Module - Randomization",
language = "en",
issn = "0737-4038",
pmid = "10605120",
doi = "10.1093/oxfordjournals.molbev.a026091"
}
@ARTICLE{Sekhon1998-hs,
title = "Genetic optimization using derivatives",
author = "Sekhon, Jasjeet S and Mebane, Walter R",
abstract = "[We describe a new computer program that combines evolutionary
algorithm methods with a derivative-based, quasi-Newton method to
solve difficult unconstrained optimization problems. The program,
called GENOUD (GENetic Optimization Using Derivatives),
effectively solves problems that are nonlinear or perhaps even
discontinuous in the parameters of the function to be optimized.
When a statistical model's estimating function (for example, a
log-likelihood) is nonlinear in the model's parameters, the
function to be optimized will usually not be globally concave and
may contain irregularities such as saddlepoints or discontinuous
jumps. Optimization methods that rely on derivatives of the
objective function may be unable to find any optimum at all. Or
multiple local optima may exist, so that there is no guarantee
that a derivative-based method will converge to the global
optimum. We discuss the theoretical basis for expecting GENOUD to
have a high probability of finding global optima. We conduct
Monte Carlo experiments using scalar Normal mixture densities to
illustrate this capability. We also use a system of four
simultaneous nonlinear equations that has many parameters and
multiple local optima to compare the performance of GENOUD to
that of the Gauss-Newton algorithm in SAS's PROC MODEL.]",
journal = "Polit. Anal.",
volume = 7,
pages = "187--210",
year = 1998,
url = "https://www.cambridge.org/core/journals/political-analysis/article/genetic-optimization-using-derivatives/9C2ACCE0EF8AA8E7E905DC4130D9660D",
keywords = "Genetic algorithm;Module - Randomization",
issn = "1047-1987, 1476-4989",
doi = "10.1093/pan/7.1.187"
}
@BOOK{Goldberg1989-zk,
title = "Genetic Algorithms in Search, Optimization, and Machine Learning",
author = "Goldberg, David E",
publisher = "Addison-Wesley",
year = 1989,
keywords = "Genetic algorithm;Module - Randomization"
}
@INPROCEEDINGS{Grefenstette1989-qz,
title = "How Genetic Algorithms Work: A Critical Look at Implicit
Parallelism",
booktitle = "Proceedings of the third international conference on Genetic
algorithms",
author = "Grefenstette, John J and Baker, James E",
pages = "20--27",
year = 1989,
keywords = "Genetic algorithm;Module - Randomization"
}
@BOOK{Holland1975-nz,
title = "Adaptation in Natural and Artificial Systems: An Introductory
Analysis with Applications to Biology, Control, and Artificial
Intelligence",
author = "Holland, John Henry",
abstract = "Genetic algorithms are playing an increasingly important role in
studies of complex adaptive systems, ranging from adaptive
agents in economic theory to the use of machine learning
techniques in the design of complex devices such as aircraft
turbines and integrated circuits. Adaptation in Natural and
Artificial Systems is the book that initiated this field of
study, presenting the theoretical foundations and exploring
applications. In its most familiar form, adaptation is a
biological process, whereby organisms evolve by rearranging
genetic material to survive in environments confronting them. In
this now classic work, Holland presents a mathematical model
that allows for the nonlinearity of such complex interactions.
He demonstrates the model's universality by applying it to
economics, physiological psychology, game theory, and artificial
intelligence and then outlines the way in which this approach
modifies the traditional views of mathematical genetics.
Initially applying his concepts to simply defined artificial
systems with limited numbers of parameters, Holland goes on to
explore their use in the study of a wide range of complex,
naturally occuring processes, concentrating on systems having
multiple factors that interact in nonlinear ways. Along the way
he accounts for major effects of coadaptation and coevolution:
the emergence of building blocks, or schemata, that are
recombined and passed on to succeeding generations to provide,
innovations and improvements.",
publisher = "University of Michigan Press",
year = 1975,
keywords = "Genetic algorithm;Module - Randomization",
isbn = "9780262581110"
}
@ARTICLE{Tavare1997-lg,
title = "Inferring coalescence times from {DNA} sequence data",
author = "Tavaré, S and Balding, D J and Griffiths, R C and Donnelly, P",
abstract = "The paper is concerned with methods for the estimation of the
coalescence time (time since the most recent common ancestor) of
a sample of intraspecies DNA sequences. The methods take
advantage of prior knowledge of population demography, in
addition to the molecular data. While some theoretical results
are presented, a central focus is on computational methods. These
methods are easy to implement, and, since explicit formulae tend
to be either unavailable or unilluminating, they are also more
useful and more informative in most applications. Extensions are
presented that allow for the effects of uncertainty in our
knowledge of population size and mutation rates, for variability
in population sizes, for regions of different mutation rate, and
for inference concerning the coalescence time of the entire
population. The methods are illustrated using recent data from
the human Y chromosome.",
journal = "Genetics",
volume = 145,
number = 2,
pages = "505--518",
month = feb,
year = 1997,
url = "https://www.ncbi.nlm.nih.gov/pubmed/9071603",
keywords = "ABC;Module - Randomization",
language = "en",
issn = "0016-6731",
pmid = "9071603",
pmc = "PMC1207814"
}
@ARTICLE{Bengtsson2021-su,
title = "A unifying framework for parallel and distributed processing in
{R} using futures",
author = "Bengtsson, Henrik",
journal = "R Journal",
publisher = "The R Foundation",
volume = 13,
number = 2,
pages = "208",
year = 2021,
url = "https://journal.r-project.org/archive/2021/RJ-2021-048/index.html",
keywords = "Module - Randomization",
language = "en",
issn = "2073-4859",
doi = "10.32614/rj-2021-048"
}
@BOOK{Sisson2018-ke,
title = "Handbook of Approximate Bayesian Computation",
author = "Sisson, Scott A and Fan, Yanan and Beaumont, Mark A",
abstract = "As the world becomes increasingly complex, so do the statistical
models required to analyse the challenging problems ahead. For
the very first time in a single volume, the Handbook of
Approximate Bayesian Computation (ABC) presents an extensive
overview of the theory, practice and application of ABC methods.
These simple, but powerful statistical techniques, take Bayesian
statistics beyond the need to specify overly simplified models,
to the setting where the model is defined only as a process that
generates data. This process can be arbitrarily complex, to the
point where standard Bayesian techniques based on working with
tractable likelihood functions would not be viable. ABC methods
finesse the problem of model complexity within the Bayesian
framework by exploiting modern computational power, thereby
permitting approximate Bayesian analyses of models that would
otherwise be impossible to implement. The Handbook of ABC
provides illuminating insight into the world of Bayesian
modelling for intractable models for both experts and newcomers
alike. It is an essential reference book for anyone interested
in learning about and implementing ABC techniques to analyse
complex models in the modern world.",
publisher = "CRC Press, Taylor and Francis Group",
month = sep,
year = 2018,
url = "https://play.google.com/store/books/details?id=t969tQEACAAJ",
keywords = "ABC;Module - Randomization",
language = "en",
isbn = "9781315117195"
}
@ARTICLE{Weiss1998-ce,
title = "Inference of population history using a likelihood approach",
author = "Weiss, G and von Haeseler, A",
abstract = "We introduce an approach to revealing the likelihood of different
population histories that utilizes an explicit model of sequence
evolution for the DNA segment under study. Based on a
phylogenetic tree reconstruction method we show that a Tamura-Nei
model with heterogeneous mutation rates is a fair description of
the evolutionary process of the hypervariable region I of the
mitochondrial DNA from humans. Assuming this complex model still
allows the estimation of population history parameters, we
suggest a likelihood approach to conducting statistical inference
within a class of expansion models. More precisely, the
likelihood of the data is based on the mean pairwise differences
between DNA sequences and the number of variable sites in a
sample. The use of likelihood ratios enables comparison of
different hypotheses about population history, such as constant
population size during the past or an increase or decrease of
population size starting at some point back in time. This method
was applied to show that the population of the Basques has
expanded, whereas that of the Biaka pygmies is most likely
decreasing. The Nuu-Chah-Nulth data are consistent with a model
of constant population.",
journal = "Genetics",
volume = 149,
number = 3,
pages = "1539--1546",
month = jul,
year = 1998,
url = "http://dx.doi.org/10.1093/genetics/149.3.1539",
keywords = "ABC;Module - Randomization",
language = "en",
issn = "0016-6731",
pmid = "9649540",
doi = "10.1093/genetics/149.3.1539",
pmc = "PMC1460236"
}
@ARTICLE{Scrucca2017-yg,
title = "On Some Extensions to {GA} Package: Hybrid Optimisation,
Parallelisation and Islands Evolution",
author = "Scrucca, Luca",
abstract = "Genetic algorithms are stochastic iterative algorithms in which
a population of individuals evolve by emulating the process of
biological evolution and natural selection. The R package GA
provides a collection of general purpose functions for
optimisation using genetic algorithms. This paper describes some
enhancements recently introduced in version 3 of the package. In
particular, hybrid GAs have been implemented by including the
option to perform local searches during the evolution. This
allows to combine the power of genetic algorithms with the speed
of a local optimiser. Another major improvement is the provision
of facilities for parallel computing. Parallelisation has been
implemented using both the master-slave approach and the islands
evolution model. Several examples of usage are presented, with
both real-world data examples and benchmark functions, showing
that often high-quality solutions can be obtained more
efficiently.",
journal = "R Journal",
publisher = "The R Foundation",
volume = 9,
number = 1,
pages = "187",
year = 2017,
url = "https://journal.r-project.org/archive/2017/RJ-2017-008/index.html",
keywords = "Genetic algorithm;Module - Randomization",
language = "en",
issn = "2073-4859",
doi = "10.32614/rj-2017-008"
}