110 research outputs found
Descubriendo Patrones Craneofaciales Usando Datos Cefalométricos Multivariados para la Toma de Decisiones en Ortodoncia
Indexación: Web of Science; Scielo.The aim was to find craniofacial morphology patterns in a multivariate cephalometric database using a clustering technique. Cephalometric analysis was performed in a sample of 100 teleradiographs collected from Chilean orthodontic patients. Thirty cephalometric measurements were taken from commonly used analysis. The computed variables were used to perform a clustering analysis with the k-means algorithm to identify patterns of craniofacial morphology. The J48 decision tree was used to analyze each cluster, and the ANOVA test to determine the statistical differences between the clusters. Four clusters were found that had significant differences (P<0.001) in 24 of the 30 variables studied, suggesting that they represent different patterns of craniofacial form. Using the decision tree, 8 of the 30 variables appeared to be relevant for describing the clusters. The clustering analysis is effective in identifying different craniofacial patterns based on a multivariate database. The distinct clusters appear to be caused by differences in the compensation process of the facial structure responding to a genetically determined cranial and mandible form. The proposed method can be applied to several databases, creating specific classifications for each one of them.
KEY WORDS: Craniofacial patterns; Morphological patterns; Clustering technique; Orthodontics.RESUMEN: El objetivo fue encontrar patrones morfológicos craneofaciales, a partir de una base de datos cefalométricos multivariada, utilizando una técnica de clustering. Se realizó un análisis cefalométrico a una muestra de 100 telerradiografías pertenecientes a pacientes chilenos de ortodoncia. Treinta medidas cefalométricas obtenidas de los análisis más utilizados fueron registradas. Las variables computadas se utilizaron para realizar un análisis de clustering con el algoritmo k-medias, para identificar patrones de morfología craneofacial. El árbol de decisión J48 se utilizó para analizar cada cluster, y test de ANOVA para determinar diferencias estadísticamente significativas entre los clusters. Se encontraron cuatro clusters con diferencia estadísticamente significativas (p<0,001) en 24 de las 30 variables estudiadas, lo que sugiere que efectivamente corresponden a diferentes patrones craneofaciales. Utilizando el árbol de decisión, se pudo determinar que 8 de las 30 variables resultaron ser relevantes en la definición de los clusters. El análisis de clustering es efectivo en identificar patrones morfológicos craneofaciales usando una base de datos multivariada. Los distintos cluster encontrados, aparentemente se formarían a partir de diferencias en el proceso de compensación de la estructura facial, en respuesta a la forma mandibular genéticamente determinada. El método propuesto puede ser aplicado a múltiples bases de datos, creando clasificaciones específicas para cada una de ellas.
PALABRAS CLAVE: Patrones craneofaciales; Patrones morfológicos; Técnica de clustering; Ortodoncia.http://ref.scielo.org/qdkkz
Physics-informed neural networks for operator equations with stochastic data
We consider the computation of statistical moments to operator equations with
stochastic data. We remark that application of PINNs -- referred to as TPINNs
-- allows to solve the induced tensor operator equations under minimal changes
of existing PINNs code, and enabling handling of non-linear and time-dependent
operators. We propose two types of architectures, referred to as vanilla and
multi-output TPINNs, and investigate their benefits and limitations. Exhaustive
numerical experiments are performed; demonstrating applicability and
performance; raising a variety of new promising research avenues
h-analysis and data-parallel physics-informed neural networks
We explore the data-parallel acceleration of physics-informed machine
learning (PIML) schemes, with a focus on physics-informed neural networks
(PINNs) for multiple graphics processing units (GPUs) architectures. In order
to develop scale-robust and high-throughput PIML models for sophisticated
applications which may require a large number of training points (e.g.,
involving complex and high-dimensional domains, non-linear operators or
multi-physics), we detail a novel protocol based on -analysis and
data-parallel acceleration through the Horovod training framework. The protocol
is backed by new convergence bounds for the generalization error and the
train-test gap. We show that the acceleration is straightforward to implement,
does not compromise training, and proves to be highly efficient and
controllable, paving the way towards generic scale-robust PIML. Extensive
numerical experiments with increasing complexity illustrate its robustness and
consistency, offering a wide range of possibilities for real-world simulations
Neutral space analysis for a Boolean network model of the fission yeast cell cycle network
BackgroundInteractions between genes and their products give rise to complex circuits known as gene regulatory networks (GRN) that enable cells to process information and respond to external stimuli. Several important processes for life, depend of an accurate and context-specific regulation of gene expression, such as the cell cycle, which can be analyzed through its GRN, where deregulation can lead to cancer in animals or a directed regulation could be applied for biotechnological processes using yeast. An approach to study the robustness of GRN is through the neutral space. In this paper, we explore the neutral space of a Schizosaccharomyces pombe (fission yeast) cell cycle network through an evolution strategy to generate a neutral graph, composed of Boolean regulatory networks that share the same state sequences of the fission yeast cell cycle.ResultsThrough simulations it was found that in the generated neutral graph, the functional networks that are not in the wildtype connected component have in general a Hamming distance more than 3 with the wildtype, and more than 10 between the other disconnected functional networks. Significant differences were found between the functional networks in the connected component of the wildtype network and the rest of the network, not only at a topological level, but also at the state space level, where significant differences in the distribution of the basin of attraction for the G1 fixed point was found for deterministic updating schemes.ConclusionsIn general, functional networks in the wildtype network connected component, can mutate up to no more than 3 times, then they reach a point of no return where the networks leave the connected component of the wildtype. The proposed method to construct a neutral graph is general and can be used to explore the neutral space of other biologically interesting networks, and also formulate new biological hypotheses studying the functional networks in the wildtype network connected component
Fast-SG: an alignment-free algorithm for hybrid assembly
International audienceBackground: Long-read sequencing technologies are the ultimate solution for genome repeats, allowing near reference-level reconstructions of large genomes. However, long-read de novo assembly pipelines are computationally intense and require a considerable amount of coverage, thereby hindering their broad application to the assembly of large genomes. Alternatively, hybrid assembly methods that combine short-and long-read sequencing technologies can reduce the time and cost required to produce de novo assemblies of large genomes. Results: Here, we propose a new method, called Fast-SG, that uses a new ultrafast alignment-free algorithm specifically designed for constructing a scaffolding graph using lightweight data structures. Fast-SG can construct the graph from either short or long reads. This allows the reuse of efficient algorithms designed for short-read data and permits the definition of novel modular hybrid assembly pipelines. Using comprehensive standard datasets and benchmarks, we show how Fast-SG outperforms the state-of-the-art short-read aligners when building the scaffolding graph and can be used to extract linking information from either raw or error-corrected long reads. We also show how a hybrid assembly approach using Fast-SG with shallow long-read coverage (5X) and moderate computational resources can produce long-range and accurate reconstructions of the genomes of Arabidopsis thaliana (Ler-0) and human (NA12878). Conclusions: Fast-SG opens a door to achieve accurate hybrid long-range reconstructions of large genomes with low effort, high portability, and low cost
Clonal chromosomal mosaicism and loss of chromosome Y in elderly men increase vulnerability for SARS-CoV-2
The pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2, COVID-19) had an estimated overall case fatality ratio of 1.38% (pre-vaccination), being 53% higher in males and increasing exponentially with age. Among 9578 individuals diagnosed with COVID-19 in the SCOURGE study, we found 133 cases (1.42%) with detectable clonal mosaicism for chromosome alterations (mCA) and 226 males (5.08%) with acquired loss of chromosome Y (LOY). Individuals with clonal mosaic events (mCA and/or LOY) showed a 54% increase in the risk of COVID-19 lethality. LOY is associated with transcriptomic biomarkers of immune dysfunction, pro-coagulation activity and cardiovascular risk. Interferon-induced genes involved in the initial immune response to SARS-CoV-2 are also down-regulated in LOY. Thus, mCA and LOY underlie at least part of the sex-biased severity and mortality of COVID-19 in aging patients. Given its potential therapeutic and prognostic relevance, evaluation of clonal mosaicism should be implemented as biomarker of COVID-19 severity in elderly people. Among 9578 individuals diagnosed with COVID-19 in the SCOURGE study, individuals with clonal mosaic events (clonal mosaicism for chromosome alterations and/or loss of chromosome Y) showed an increased risk of COVID-19 lethality
Improving the performance of inductive learning classifiers through the presentation order of the training patterns
Bayesian Constitutionalization: Twitter Sentiment Analysis of the Chilean Constitutional Process through Bayesian Network Classifiers
Constitutional processes are a cornerstone of modern democracies. Whether revolutionary or institutionally organized, they establish the core values of social order and determine the institutional architecture that governs social life. Constitutional processes are themselves evolutionary practices of mutual learning in which actors, regardless of their initial political positions, continuously interact with each other, demonstrating differences and making alliances regarding different topics. In this article, we develop Tree Augmented Naive Bayes (TAN) classifiers to model the behavior of constituent agents. According to the nature of the constituent dynamics, weights are learned by the model from the data using an evolution strategy to obtain a good classification performance. For our analysis, we used the constituent agents’ communications on Twitter during the installation period of the Constitutional Convention (July–October 2021). In order to differentiate political positions (left, center, right), we applied the developed algorithm to obtain the scores of 882 ballots cast in the first stage of the convention (4 July to 29 September 2021). Then, we used k-means to identify three clusters containing right-wing, center, and left-wing positions. Experimental results obtained using the three constructed datasets showed that using alternative weight values in the TAN construction procedure, inferred by an evolution strategy, yielded improvements in the classification accuracy measured in the test sets compared to the results of the TAN constructed with conditional mutual information, as well as other Bayesian network classifier construction approaches. Additionally, our results may help us to better understand political behavior in constitutional processes and to improve the accuracy of TAN classifiers applied to social, real-world data
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