A multiple expression alignment framework for genetic programming

Dissertation presented as the partial requirement for obtaining a Master's degree in Data Science and Advanced AnalyticsAlignment in the error space is a recent idea to exploit semantic awareness in genetic programming. In a previous contribution, the concepts of optimally aligned and optimally coplanar individuals were introduced, and it was shown that given optimally aligned, or optimally coplanar, individuals, it is possible to construct a globally optimal solution analytically. Consequently, genetic programming methods, aimed at searching for optimally aligned, or optimally coplanar, individuals were introduced. This paper critically discusses those methods, analyzing their major limitations and introduces a new genetic programming system aimed at overcoming those limitations. The presented experimental results, conducted on five real-life symbolic regression problems, show that the proposed algorithms’ outperform not only the existing methods based on the concept of alignment in the error space, but also geometric semantic genetic programming and standard genetic programming

A multiple expression alignment framework for genetic programming

Vanneschi, L., Scott, K., & Castelli, M. (2018). A multiple expression alignment framework for genetic programming. In M. Castelli, L. Sekanina, M. Zhang, S. Cagnoni, & P. García-Sánchez (Eds.), Genetic Programming: 21st European Conference, EuroGP 2018, Proceedings, pp. 166-183. (Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics); Vol. 10781 LNCS). Springer Verlag. DOI: 10.1007/978-3-319-77553-1_11Alignment in the error space is a recent idea to exploit semantic awareness in genetic programming. In a previous contribution, the concepts of optimally aligned and optimally coplanar individuals were introduced, and it was shown that given optimally aligned, or optimally coplanar, individuals, it is possible to construct a globally optimal solution analytically. As a consequence, genetic programming methods, aimed at searching for optimally aligned, or optimally coplanar, individuals were introduced. In this paper, we critically discuss those methods, analyzing their major limitations and we propose new genetic programming systems aimed at overcoming those limitations. The presented experimental results, conducted on four real-life symbolic regression problems, show that the proposed algorithms outperform not only the existing methods based on the concept of alignment in the error space, but also geometric semantic genetic programming and standard genetic programming.authorsversionpublishe

Developing and applying heterogeneous phylogenetic models with XRate

Modeling sequence evolution on phylogenetic trees is a useful technique in computational biology. Especially powerful are models which take account of the heterogeneous nature of sequence evolution according to the "grammar" of the encoded gene features. However, beyond a modest level of model complexity, manual coding of models becomes prohibitively labor-intensive. We demonstrate, via a set of case studies, the new built-in model-prototyping capabilities of XRate (macros and Scheme extensions). These features allow rapid implementation of phylogenetic models which would have previously been far more labor-intensive. XRate's new capabilities for lineage-specific models, ancestral sequence reconstruction, and improved annotation output are also discussed. XRate's flexible model-specification capabilities and computational efficiency make it well-suited to developing and prototyping phylogenetic grammar models. XRate is available as part of the DART software package: http://biowiki.org/DART .Comment: 34 pages, 3 figures, glossary of XRate model terminolog

The EM Algorithm and the Rise of Computational Biology

In the past decade computational biology has grown from a cottage industry with a handful of researchers to an attractive interdisciplinary field, catching the attention and imagination of many quantitatively-minded scientists. Of interest to us is the key role played by the EM algorithm during this transformation. We survey the use of the EM algorithm in a few important computational biology problems surrounding the "central dogma"; of molecular biology: from DNA to RNA and then to proteins. Topics of this article include sequence motif discovery, protein sequence alignment, population genetics, evolutionary models and mRNA expression microarray data analysis.Comment: Published in at http://dx.doi.org/10.1214/09-STS312 the Statistical Science (http://www.imstat.org/sts/) by the Institute of Mathematical Statistics (http://www.imstat.org

Parametric inference of recombination in HIV genomes

Recombination is an important event in the evolution of HIV. It affects the global spread of the pandemic as well as evolutionary escape from host immune response and from drug therapy within single patients. Comprehensive computational methods are needed for detecting recombinant sequences in large databases, and for inferring the parental sequences. We present a hidden Markov model to annotate a query sequence as a recombinant of a given set of aligned sequences. Parametric inference is used to determine all optimal annotations for all parameters of the model. We show that the inferred annotations recover most features of established hand-curated annotations. Thus, parametric analysis of the hidden Markov model is feasible for HIV full-length genomes, and it improves the detection and annotation of recombinant forms. All computational results, reference alignments, and C++ source code are available at http://bio.math.berkeley.edu/recombination/.Comment: 20 pages, 5 figure

Updates in metabolomics tools and resources: 2014-2015

Data processing and interpretation represent the most challenging and time-consuming steps in high-throughput metabolomic experiments, regardless of the analytical platforms (MS or NMR spectroscopy based) used for data acquisition. Improved machinery in metabolomics generates increasingly complex datasets that create the need for more and better processing and analysis software and in silico approaches to understand the resulting data. However, a comprehensive source of information describing the utility of the most recently developed and released metabolomics resources—in the form of tools, software, and databases—is currently lacking. Thus, here we provide an overview of freely-available, and open-source, tools, algorithms, and frameworks to make both upcoming and established metabolomics researchers aware of the recent developments in an attempt to advance and facilitate data processing workflows in their metabolomics research. The major topics include tools and researches for data processing, data annotation, and data visualization in MS and NMR-based metabolomics. Most in this review described tools are dedicated to untargeted metabolomics workflows; however, some more specialist tools are described as well. All tools and resources described including their analytical and computational platform dependencies are summarized in an overview Table

Regulatory motif discovery using a population clustering evolutionary algorithm

This paper describes a novel evolutionary algorithm for regulatory motif discovery in DNA promoter sequences. The algorithm uses data clustering to logically distribute the evolving population across the search space. Mating then takes place within local regions of the population, promoting overall solution diversity and encouraging discovery of multiple solutions. Experiments using synthetic data sets have demonstrated the algorithm's capacity to find position frequency matrix models of known regulatory motifs in relatively long promoter sequences. These experiments have also shown the algorithm's ability to maintain diversity during search and discover multiple motifs within a single population. The utility of the algorithm for discovering motifs in real biological data is demonstrated by its ability to find meaningful motifs within muscle-specific regulatory sequences