Práctica de desarrollo de interfaces hardware/software para la monitorización del estado de un PC

Este artículo presenta una práctica laboratorio impartida mediante una metodología de aprendizaje basado en proyectos (ABP) [1] para dotar de la capacidad de diseñar y desarrollar un monitor del estado de un ordenador, integrado en un sistema empotrado que se comunica con una aplicación de escritorio, a nuestros alumnos de la asignatura de Diseño de Microcontroladores (DM) en el contexto del Máster en Ingeniería de Computadores y Redes. Esta práctica abarca la comunicación Hardware/ Software entre un microcontrolador con un núcleo Cortex-M4 y una aplicación software escrita en lenguaje C# usando el entorno Visual Studio Community 2015 a través de puertos series virtuales (VCP). Esta práctica está enfocada como un proyecto que los alumnos han de ir realizando desde cero, avanzando mediante la consecución de hitos, hasta conseguir obtener un sistema final. El sistema a desarrollar se divide en dos partes, por un lado tenemos un PC con un sistema operativo de la familia Windows, en el que se construye una aplicación visual mediante Windows Forms, la cual obtiene información del sistema de forma periódica y la envía al microcontrolador mediante comandos usando el puerto serie (USB o comunicación Bluetooth). Por otro lado tenemos un microcontrolador de la familia STM32 que dispone de un display LCD ejecutando una plataforma completamente libre, .NET Micro Framework, la cual recibe a través del puerto serie la información obtenida gracias a la aplicación software del PC y la muestra en la pantalla, obteniendo así una herramienta de monitorización del PC sin tener que estar conectado físicamente a éste. El desarrollo de este tipo de proyectos se añade la dificultad de la necesidad del uso de diferentes herramientas para el desarrollo del firmware y del software en paralelo, de manera incremental, y enfocadas para ámbitos de uso muy distintos. Esta práctica ha tenido una gran acogida por parte de los alumnos, ya que les ha servido de ejemplo del desarrollo de firmware para un microcontrolador usando la plataforma .NET MF y de su comunicación con el PC por medio de una aplicación visual.This manuscript presents a practical laboratory session imparted using a project-based learning methodology (PBL) to provide the capacity of designing and developing a computer status monitoring device, integrated in an embedded system that communicates with a desktop software tool, to our students in the Computer Engineering Master’s Degree. This practice session encompasses Hardware/ Software communication between a microcontroller with a Cortex-M4 kernel and a desktop software application through virtual COM ports (VCP) written in C# using Visual Studio Community 2015. This lab session is focused as a project that students must be making from scratch by achieving and completing some milestones to obtain a final functional system. The project is divided into two different parts. First, we have a Windows PC where a visual software application that gathers information from the system and sends it periodically to the microcontroller (USB or Bluetooth) has to be built using Windows Forms. On the other hand, we have a microcontroller from the STM32 family that has a 2.4’ LCD display executing .NET Micro Framework that receives the information obtained from the PC through the serial port and displays it in the screen. This way, students create a computer status monitoring tool that does not need to be connected physically to it to receive the information. The development of this project is added to the need of using different tools for firmware and software development, focused to very different fields of use. This practice has been well received by the students, because it has served as an example of the firmware development for a microcontroller using the .NET MF platform as well as the communication between the PC and the microcontroller using a visual software application

Live Demonstration:Neuromorphic Sensory Integration for Combining Sound Source Localization and Collision Avoidance

The brain is able to solve complex tasks in real time by combining different sensory cues with previously acquired knowledge. Inspired by the brain, we designed a neuromorphic demonstrator which combines auditory and visual input to find an obstacle free direction closest to the sound source. The system consists of two event-based sensors (the eDVS for vision and the NAS for audition) mounted onto a pan-tilt unit and a spiking neural network implemented on the SpiNNaker platform. By combining the different sensory information, the demonstrator is able to point at a sound source direction while avoiding obstacles in real time

Feature Extraction and Random Forest to Identify Sheep Behavior from Accelerometer Data

Sensor technologies play an essential part in the agricultural community and many other scientific and commercial communities. Accelerometer signals and Machine Learning techniques can be used to identify and observe behaviours of animals without the need for an exhaustive human observation which is labour intensive and time consuming. This study employed random forest algorithm to identify grazing, walking, scratching, and inactivity (standing, resting) of 8 Hebridean ewes located in Cheshire, Shotwick in the UK. We gathered accelerometer data from a sensor device which was fitted on the collar of the animals. The selection of the algorithm was based on previous research by which random forest achieved the best results among other benchmark techniques. Therefore, in this study, more focus was given to feature engineering to improve prediction performance. Seventeen features from time and frequency domain were calculated from the accelerometer measurements and the magnitude of the acceleration. Feature elimination was utilised in which highly correlated ones were removed, and only nine out of seventeen features were selected. The algorithm achieved an overall accuracy of 99.43% and a kappa value of 98.66%. The accuracy for grazing, walking, scratching, and inactive was 99.08%, 99.13%, 99.90%, and 99.85%, respectively. The overall results showed that there is a significant improvement over previous methods and studies for all mutually exclusive behaviours. Those results are promising, and the technique could be further tested for future real-time activity recognition

Functional Characterization of MODY2 Mutations Highlights the Importance of the Fine-Tuning of Glucokinase and Its Role in Glucose Sensing

Glucokinase (GK) acts as a glucose sensor in the pancreatic beta-cell and regulates insulin secretion. Heterozygous mutations in the human GK-encoding GCK gene that reduce the activity index increase the glucose-stimulated insulin secretion threshold and cause familial, mild fasting hyperglycaemia, also known as Maturity Onset Diabetes of the Young type 2 (MODY2). Here we describe the biochemical characterization of five missense GK mutations: p.Ile130Thr, p.Asp205His, p.Gly223Ser, p.His416Arg and p.Ala449Thr. The enzymatic analysis of the corresponding bacterially expressed GST-GK mutant proteins show that all of them impair the kinetic characteristics of the enzyme. In keeping with their position within the protein, mutations p.Ile130Thr, p.Asp205His, p.Gly223Ser, and p.His416Arg strongly decrease the activity index of GK, affecting to one or more kinetic parameters. In contrast, the p.Ala449Thr mutation, which is located in the allosteric activator site, does not affect significantly the activity index of GK, but dramatically modifies the main kinetic parameters responsible for the function of this enzyme as a glucose sensor. The reduced Kcat of the mutant (3.21±0.28 s−1 vs 47.86±2.78 s−1) is balanced by an increased glucose affinity (S0.5 = 1.33±0.08 mM vs 7.86±0.09 mM) and loss of cooperativity for this substrate. We further studied the mechanism by which this mutation impaired GK kinetics by measuring the differential effects of several competitive inhibitors and one allosteric activator on the mutant protein. Our results suggest that this mutation alters the equilibrium between the conformational states of glucokinase and highlights the importance of the fine-tuning of GK and its role in glucose sensing

X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients

Rett syndrome (RTT) is a severe neurological disorder usually caused by mutations in the MECP2 gene. Since the MECP2 gene is located on the X chromosome, X chromosome inactivation (XCI) could play a role in the wide range of phenotypic variation of RTT patients; however, classical methylation-based protocols to evaluate XCI could not determine whether the preferentially inactivated X chromosome carried the mutant or the wild-type allele. Therefore, we developed an allele-specific methylation-based assay to evaluate methylation at the loci of several recurrent MECP2 mutations. We analyzed the XCI patterns in the blood of 174 RTT patients, but we did not find a clear correlation between XCI and the clinical presentation. We also compared XCI in blood and brain cortex samples of two patients and found differences between XCI patterns in these tissues. However, RTT mainly being a neurological disease complicates the establishment of a correlation between the XCI in blood and the clinical presentation of the patients. Furthermore, we analyzed MECP2 transcript levels and found differences from the expected levels according to XCI. Many factors other than XCI could affect the RTT phenotype, which in combination could influence the clinical presentation of RTT patients to a greater extent than slight variations in the XCI pattern

Viruses and Mycoplasma pneumoniae are the main etiological agents of community-acquired pneumonia in hospitalized pediatric patients in Spain

[Objectives]: To describe the etiology of community-acquired pneumonia (CAP) in hospitalized children in Spain and analyze the predictors of the etiology.[Hypothesis]: The different etiological groups of pediatric CAP are associated with different clinical, radiographic, and analytical data.[Design]: Observational, multicenter, and prospective study.[Patient selection]: This study included children aged 1 month to 17 years with CAP, who were hospitalized between April 2012 and May 2019.[Methods]: An extensive microbiological workup was performed. The clinical, radiographic, and analytical parameters were analyzed for three etiological groups.[Results]: Among the 495 children included, at least one causative pathogen was identified in 262 (52.9%): pathogenic viruses in 155/262 (59.2%); atypical bacteria (AB), mainly Mycoplasma pneumonia, in 84/262 (32.1%); and typical bacteria (TyB) in 40/262 (15.3%). Consolidation was observed in 89/138 (64.5%) patients with viral CAP, 74/84 (88.1%) with CAP caused by AB, and 40/40 (100%) with CAP caused by TyB. Para-pneumonic pleural effusion (PPE) was observed in 112/495 (22.6%) patients, of which 61/112 (54.5%) presented a likely causative pathogen: viruses in 12/61 (19.7%); AB in 23/61 (37.7%); and TyB in 26/61 (42.6%). Viral etiology was significantly frequent in young patients and in those with low oxygen saturation, wheezing, no consolidation, and high lymphocyte counts. CAP patients with AB as the etiological agent had a significantly longer and less serious course as compared to those with other causative pathogens.[Conclusions]: Viruses and M. pneumoniae are the main causes of pediatric CAP in Spain. Wheezing, young age, and no consolidation on radiographs are indicative of viral etiology. Viruses and AB can also cause PPE. Since only a few cases can be directly attributed to TyB, the indications for antibiotics must be carefully considered in each patient.Instituto de Investigación Hospital 12 de Octubre (i+12), Grant/Award Number: AY191212‐1; Instituto de Salud Carlos III (Ministry of Economy, Industry and Competitiveness) and co‐funded by the European Regional Development Funds, Grant/Award Number: Project PI17/01458; Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Grant/Award Number: PCAPE 2011_0025 Register 320/11; Research Project of Universidad Europea de Madrid, Grant/Award Number: 2017/UEM03Peer reviewe

Impact of COVID-19 pandemic on cardiovascular testing in Asia: the IAEA INCAPS-COVID study

BACKGROUND The coronavirus disease-2019 (COVID-19) pandemic significantly affected management of cardiovascular disease around the world. The effect of the pandemic on volume of cardiovascular diagnostic procedures is not known. OBJECTIVES This study sought to evaluate the effects of the early phase of the COVID-19 pandemic on cardiovascular diagnostic procedures and safety practices in Asia. METHODS The International Atomic Energy Agency conducted a worldwide survey to assess changes in cardiovascular procedure volume and safety practices caused by COVID-19. Testing volumes were reported for March 2020 and April 2020 and were compared to those from March 2019. Data from 180 centers across 33 Asian countries were grouped into 4 subregions for comparison. RESULTS Procedure volumes decreased by 47% from March 2019 to March 2020, showing recovery from March 2020 to April 2020 in Eastern Asia, particularly in China. The majority of centers cancelled outpatient activities and increased time per study. Practice changes included implementing physical distancing and restricting visitors. Although COVID testing was not commonly performed, it was conducted in one-third of facilities in Eastern Asia. The most severe reductions in procedure volumes were observed in lower-income countries, where volumes decreased 81% from March 2019 to April 2020. CONCLUSIONS The COVID-19 pandemic in Asia caused significant reductions in cardiovascular diagnostic procedures, particularly in low-income countries. Further studies on effects of COVID-19 on cardiovascular outcomes and changes in care delivery are warranted

Geographical and temporal distribution of SARS-CoV-2 clades in the WHO European Region, January to June 2020

We show the distribution of SARS-CoV-2 genetic clades over time and between countries and outline potential genomic surveillance objectives. We applied three available genomic nomenclature systems for SARS-CoV-2 to all sequence data from the WHO European Region available during the COVID-19 pandemic until 10 July 2020. We highlight the importance of real-time sequencing and data dissemination in a pandemic situation. We provide a comparison of the nomenclatures and lay a foundation for future European genomic surveillance of SARS-CoV-2.Peer reviewe