102 research outputs found
Applying recursive modelling to assess the role of the host genome and the gut microbiome on feed efficiency in pigs
The gut microbiome plays an important role in the performance and health of swine by providing essential nutrients and supporting the immune system. Recent studies have demonstrated that the gut microbiome can explain part of the variation observed in growth, health, and meat quality. Feed efficiency is crucial in swine production, as feed cost account for more than 60% of total production costs. This study aimed to assess the relationships between the host genome, gut microbiome, and feed efficiency in Iberian pigs raised under intensive conditions. The specific objectives were to assess the mediating effects of the gut microbiome on feed efficiency and to estimate the direct and total heritability of feed efficiency. The data set included the feed conversion ratio (FCR) and residual feed intake (RFI) from 587 Iberian pigs, as well as the 16S rRNA gut microbial abundance from 151 of those pigs raised in a nucleus of selection. We reparametrised variance components from standard bivariate mixed models into recursive models to disentangle the microbiomeâs mediating effect on feed efficiency. In our models, the host genome has direct effects on both the phenotype (GâP) and the gut microbiome (GâM). Additionally, there is an indirect effect of the host genome on the phenotype mediated by the microbiome (GâMâP). We identified a total of 14 taxa with relevant effects on FCR and 16 taxa with relevant effects on RFI. We categorised the gut microbiome into groups for potential practical application in pig farming. The gut microbes with relevant causal effects and low heritability can be manipulated through management interventions, while those microbes with relevant causal effects and moderate heritability can be targeted through selective breeding. Our findings indicate that incorporating microbiome data leads to a reduction in total heritability for both FCR and RFI. This study provides new insights into the link between the gut microbiome and feed efficiency, presenting practical methods to target microbes that can be influenced through selective breeding or management interventions
The R Journal (December 2012) 4(2): Complete Issue
Contributing Articles
What\u27s in a Name? Paul Murrell
It\u27s Not What You Draw, It\u27s What You Don\u27t Draw, Paul Murrell
Debugging grid Graphics, Paul Murrell and Velvet Ly
frailtyHL: A Package for Fitting Frailty Models with H-likelihood, Il Do Ha, Maengseok Noh, and Youngjo Lee
influence.ME: Tools for Detecting Influential Data in Mixed Effects Models, Rense Nieuwenhuis, Manfred te Grotenhuis and Ben Pelzer
The crs Package: Nonparametric Regression Splines for Continuous and Categorical Predictors, Zhenghua Nie and Jeffrey S. Racine
Rfit: Rank-based Estimation for Linear Models, John D. Kloke and Joseph W. McKean
Graphical Markov Models with Mixed Graphs in R, Kayvan Sadeghi and Giovanni M. Marchetti
The State of Naming Conventions in R, Rasmus BÄÄth
News and notes
Changes in R
Changes on CRA
News from the Bioconductor Project
R Foundation New
Heart Diseases Diagnosis Using Artificial Neural Networks
Information technology has virtually altered every aspect of human life in the present era. The application of informatics in the health sector is rapidly gaining prominence and the benefits of this innovative paradigm are being realized across the globe. This evolution produced large number of patientsâ data that can be employed by computer technologies and machine learning techniques, and turned into useful information and knowledge. This data can be used to develop expert systems to help in diagnosing some life-threating diseases such as heart diseases, with less cost, processing time and improved diagnosis accuracy. Even though, modern medicine is generating huge amount of data every day, little has been done to use this available data to solve challenges faced in the successful diagnosis of heart diseases. Highlighting the need for more research into the usage of robust data mining techniques to help health care professionals in the diagnosis of heart diseases and other debilitating disease conditions.
Based on the foregoing, this thesis aims to develop a health informatics system for the classification of heart diseases using data mining techniques focusing on Radial Basis functions and emerging Neural Networks approach. The presented research involves three development stages; firstly, the development of a preliminary classification system for Coronary Artery Disease (CAD) using Radial Basis Function (RBF) neural networks. The research then deploys the deep learning approach to detect three different types of heart diseases i.e. Sleep Apnea, Arrhythmias and CAD by designing two novel classification systems; the first adopt a novel deep neural network method (with Rectified Linear unit activation) design as the second approach in this thesis and the other implements a novel multilayer kernel machine to mimic the behaviour of deep learning as the third approach. Additionally, this thesis uses a dataset obtained from patients, and employs normalization and feature extraction means to explore it in a unique way that facilitates its usage for training and validating different classification methods. This unique dataset is useful to researchers and practitioners working in heart disease treatment and diagnosis.
The findings from the study reveal that the proposed models have high classification performance that is comparable, or perhaps exceed in some cases, the existing automated and manual methods of heart disease diagnosis. Besides, the proposed deep-learning models provide better performance when applied on large data sets (e.g., in the case of Sleep Apnea), with reasonable performance with smaller data sets.
The proposed system for clinical diagnoses of heart diseases, contributes to the accurate detection of such disease, and could serve as an important tool in the area of clinic support system. The outcome of this study in form of implementation tool can be used by cardiologists to help them make more consistent diagnosis of heart diseases
Using genetic markers to orient the edges in quantitative trait networks: The NEO software
<p>Abstract</p> <p>Background</p> <p>Systems genetic studies have been used to identify genetic loci that affect transcript abundances and clinical traits such as body weight. The pairwise correlations between gene expression traits and/or clinical traits can be used to define undirected trait networks. Several authors have argued that genetic markers (e.g expression quantitative trait loci, eQTLs) can serve as causal anchors for orienting the edges of a trait network. The availability of hundreds of thousands of genetic markers poses new challenges: how to relate (anchor) traits to multiple genetic markers, how to score the genetic evidence in favor of an edge orientation, and how to weigh the information from multiple markers.</p> <p>Results</p> <p>We develop and implement Network Edge Orienting (NEO) methods and software that address the challenges of inferring unconfounded and directed gene networks from microarray-derived gene expression data by integrating mRNA levels with genetic marker data and Structural Equation Model (SEM) comparisons. The NEO software implements several manual and automatic methods for incorporating genetic information to anchor traits. The networks are oriented by considering each edge separately, thus reducing error propagation. To summarize the genetic evidence in favor of a given edge orientation, we propose Local SEM-based Edge Orienting (LEO) scores that compare the fit of several competing causal graphs. SEM fitting indices allow the user to assess local and overall model fit. The NEO software allows the user to carry out a robustness analysis with regard to genetic marker selection. We demonstrate the utility of NEO by recovering known causal relationships in the sterol homeostasis pathway using liver gene expression data from an F2 mouse cross. Further, we use NEO to study the relationship between a disease gene and a biologically important gene co-expression module in liver tissue.</p> <p>Conclusion</p> <p>The NEO software can be used to orient the edges of gene co-expression networks or quantitative trait networks if the edges can be anchored to genetic marker data. R software tutorials, data, and supplementary material can be downloaded from: <url>http://www.genetics.ucla.edu/labs/horvath/aten/NEO</url>.</p
Artificial Intelligence and Machine Learning in Health Care and Medical Sciences
This open access book provides a detailed review of the latest methods and applications of artificial intelligence (AI) and machine learning (ML) in medicine. With chapters focusing on enabling the reader to develop a thorough understanding of the key concepts in these subject areas along with a range of methods and resulting models that can be utilized to solve healthcare problems, the use of causal and predictive models are comprehensively discussed. Care is taken to systematically describe the concepts to facilitate the reader in developing a thorough conceptual understanding of how different methods and resulting models function and how these relate to their applicability to various issues in health care and medical sciences. Guidance is also given on how to avoid pitfalls that can be encountered on a day-to-day basis and stratify potential clinical risks. Artificial Intelligence and Machine Learning in Health Care and Medical Sciences: Best Practices and Pitfallsis a comprehensive guide to how AI and ML techniques can best be applied in health care. The emphasis placed on how to avoid a variety of pitfalls that can be encountered makes it an indispensable guide for all medical informatics professionals and physicians who utilize these methodologies on a day-to-day basis. Furthermore, this work will be of significant interest to health data scientists, administrators and to students in the health sciences seeking an up-to-date resource on the topic
Proceedings of the 24th Conference on Formal Methods in Computer-Aided Design â FMCAD 2024
The Conference on Formal Methods in Computer-Aided Design (FMCAD) is an annual conference on the theory and applications of formal methods in hardware and system in academia and industry for presenting and discussing groundbreaking methods, technologies, theoretical results, and tools for reasoning formally about computing systems. FMCAD covers formal aspects of computer-aided system testing
Scalable Logic Defined Static Analysis
Logic languages such as Datalog have been proposed as a method for specifying flexible and customisable static analysers. Using Datalog, various classes of static analyses can be expressed precisely and succinctly, requiring fewer lines of code than hand-crafted analysers. In this paradigm, a static analysis specification is encoded by a set of declarative logic rules and an o -the-shelf solver is used to compute the result of the static analysis. Unfortunately, when large-scale analyses are employed, Datalog-based tools currently fail to scale in comparison to hand-crafted static analysers. As a result, Datalog-based analysers have largely remained an academic curiosity, rather than industrially respectful tools. This thesis outlines our e orts in understanding the sources of performance limitations in Datalog-based tools. We propose a novel evaluation technique that is predicated on the fact that in the case of static analysis, the logical specification is a design time artefact and hence does not change during evaluation. Thus, instead of directly evaluating Datalog rules, our approach leverages partial evaluation to synthesise a specialised static analyser from these rules. This approach enables a novel indexing optimisations that automatically selects an optimal set of indexes to speedup and minimise memory usage in the Datalog computation. Lastly, we explore the case of more expressive logics, namely, constrained Horn clause and their use in proving the correctness of programs. We identify a bottleneck in various symbolic evaluation algorithms that centre around Craig interpolation. We propose a method of improving these evaluation algorithms by a proposing a method of guiding theorem provers to discover relevant interpolants with respect to the input logic specification. The culmination of our work is implemented in a general-purpose and highperformance tool called SoufflÂŽe. We describe SoufflÂŽe and evaluate its performance experimentally, showing significant improvement over alternative techniques and its scalability in real-world industrial use cases
PSA 2018
These preprints were automatically compiled into a PDF from the collection of papers deposited in PhilSci-Archive in conjunction with the PSA 2018
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