11,167 research outputs found

    On the design of diploid genetic algorithms for problem optimization in dynamic environments

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    Tihis article is posted here with permission from the IEEE - Copyright @ 2006 IEEEUsing diploidy and dominance is one method to enhance the performance of genetic algorithms in dynamic environments. For diploidy genetic algorithms, there are two key design factors: the cardinality of genotypic alleles and the uncertainty in the dominance scheme. This paper investigates the effect of these two factors on the performance of diploidy genetic algorithms in dynamic environments. A generalized diploidy and dominance scheme is proposed for diploidy genetic algorithms, where the cardinality of genotypic alleles and/or the uncertainty in the dominance scheme can be easily tuned and studied. The experimental results show the efficiency of increasing genotypic cardinality rather than introducing uncertainty in the dominance scheme

    Compressed Genotyping

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    Significant volumes of knowledge have been accumulated in recent years linking subtle genetic variations to a wide variety of medical disorders from Cystic Fibrosis to mental retardation. Nevertheless, there are still great challenges in applying this knowledge routinely in the clinic, largely due to the relatively tedious and expensive process of DNA sequencing. Since the genetic polymorphisms that underlie these disorders are relatively rare in the human population, the presence or absence of a disease-linked polymorphism can be thought of as a sparse signal. Using methods and ideas from compressed sensing and group testing, we have developed a cost-effective genotyping protocol. In particular, we have adapted our scheme to a recently developed class of high throughput DNA sequencing technologies, and assembled a mathematical framework that has some important distinctions from 'traditional' compressed sensing ideas in order to address different biological and technical constraints.Comment: Submitted to IEEE Transaction on Information Theory - Special Issue on Molecular Biology and Neuroscienc

    Fast Identification of Biological Pathways Associated with a Quantitative Trait Using Group Lasso with Overlaps

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    Where causal SNPs (single nucleotide polymorphisms) tend to accumulate within biological pathways, the incorporation of prior pathways information into a statistical model is expected to increase the power to detect true associations in a genetic association study. Most existing pathways-based methods rely on marginal SNP statistics and do not fully exploit the dependence patterns among SNPs within pathways. We use a sparse regression model, with SNPs grouped into pathways, to identify causal pathways associated with a quantitative trait. Notable features of our "pathways group lasso with adaptive weights" (P-GLAW) algorithm include the incorporation of all pathways in a single regression model, an adaptive pathway weighting procedure that accounts for factors biasing pathway selection, and the use of a bootstrap sampling procedure for the ranking of important pathways. P-GLAW takes account of the presence of overlapping pathways and uses a novel combination of techniques to optimise model estimation, making it fast to run, even on whole genome datasets. In a comparison study with an alternative pathways method based on univariate SNP statistics, our method demonstrates high sensitivity and specificity for the detection of important pathways, showing the greatest relative gains in performance where marginal SNP effect sizes are small.Comment: 29 page

    Routes for breaching and protecting genetic privacy

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    We are entering the era of ubiquitous genetic information for research, clinical care, and personal curiosity. Sharing these datasets is vital for rapid progress in understanding the genetic basis of human diseases. However, one growing concern is the ability to protect the genetic privacy of the data originators. Here, we technically map threats to genetic privacy and discuss potential mitigation strategies for privacy-preserving dissemination of genetic data.Comment: Draft for comment
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