417 research outputs found

    State-dependent complexity of the local field potential in the primary visual cortex

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    The local field potential (LFP) is as a measure of the combined activity of neurons within a region of brain tissue. While biophysical modeling schemes for LFP in cortical circuits are well established, there is a paramount lack of understanding regarding the LFP properties along the states assumed in cortical circuits over long periods. Here we use a symbolic information approach to determine the statistical complexity based on Jensen disequilibrium measure and Shannon entropy of LFP data recorded from the primary visual cortex (V1) of urethane-anesthetized rats and freely moving mice. Using these information quantifiers, we find consistent relations between LFP recordings and measures of cortical states at the neuronal level. More specifically, we show that LFP's statistical complexity is sensitive to cortical state (characterized by spiking variability), as well as to cortical layer. In addition, we apply these quantifiers to characterize behavioral states of freely moving mice, where we find indirect relations between such states and spiking variability

    SIMBA: a web tool for managing bacterial genome assembly generated by Ion PGM sequencing technology

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    Background The evolution of Next-Generation Sequencing (NGS) has considerably reduced the cost per sequenced-base, allowing a significant rise of sequencing projects, mainly in prokaryotes. However, the range of available NGS platforms requires different strategies and software to correctly assemble genomes. Different strategies are necessary to properly complete an assembly project, in addition to the installation or modification of various software. This requires users to have significant expertise in these software and command line scripting experience on Unix platforms, besides possessing the basic expertise on methodologies and techniques for genome assembly. These difficulties often delay the complete genome assembly projects. Results In order to overcome this, we developed SIMBA (SImple Manager for Bacterial Assemblies), a freely available web tool that integrates several component tools for assembling and finishing bacterial genomes. SIMBA provides a friendly and intuitive user interface so bioinformaticians, even with low computational expertise, can work under a centralized administrative control system of assemblies managed by the assembly center head. SIMBA guides the users to execute assembly process through simple and interactive pages. SIMBA workflow was divided in three modules: (i) projects: allows a general vision of genome sequencing projects, in addition to data quality analysis and data format conversions; (ii) assemblies: allows de novo assemblies with the software Mira, Minia, Newbler and SPAdes, also assembly quality validations using QUAST software; and (iii) curation: presents methods to finishing assemblies through tools for scaffolding contigs and close gaps. We also presented a case study that validated the efficacy of SIMBA to manage bacterial assemblies projects sequenced using Ion Torrent PGM. Conclusion Besides to be a web tool for genome assembly, SIMBA is a complete genome assemblies project management system, which can be useful for managing of several projects in laboratories. SIMBA source code is available to download and install in local webservers at http://ufmg-simba.sourceforge.net

    Genomics and epidemiology of the P.1 SARS-CoV-2 lineage in Manaus, Brazil

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    Cases of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in Manaus, Brazil, resurged in late 2020 despite previously high levels of infection. Genome sequencing of viruses sampled in Manaus between November 2020 and January 2021 revealed the emergence and circulation of a novel SARS-CoV-2 variant of concern. Lineage P.1 acquired 17 mutations, including a trio in the spike protein (K417T, E484K, and N501Y) associated with increased binding to the human ACE2 (angiotensin-converting enzyme 2) receptor. Molecular clock analysis shows that P.1 emergence occurred around mid-November 2020 and was preceded by a period of faster molecular evolution. Using a two-category dynamical model that integrates genomic and mortality data, we estimate that P.1 may be 1.7- to 2.4-fold more transmissible and that previous (non-P.1) infection provides 54 to 79% of the protection against infection with P.1 that it provides against non-P.1 lineages. Enhanced global genomic surveillance of variants of concern, which may exhibit increased transmissibility and/or immune evasion, is critical to accelerate pandemic responsiveness

    Redes neurais artificiais aplicadas na previsão do VTEC no Brasil

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    Uma forma de se prever o conteúdo total de elétrons na direção vertical (VTEC - Vertical Total Electron Content) usando a arquitetura de redes neurais artificiais (RNA) denominada de perceptrons de múltiplas camadas (MLP - MultipLayer Percetrons) é apresentada e avaliada nesta pesquisa. As entradas do modelo foram definidas como sendo a posição dos pontos ionosféricos (IPP - Ionospheric Pierce Point) e o tempo universal (TU), enquanto que a saída é o VTEC. As variações sazonais e de períodos mais longos são levadas em conta através da atualização do treinamento diariamente. Testes foram conduzidos sobre uma área que abrange o Brasil e sua vizinhança considerando períodos de alta e baixa atividade solar. As RNA foram treinadas utilizando informações dos mapas globais da ionosfera (GIM - Global Ionospheric Maps) produzidos pelo serviço internacional do GNSS (IGS - International GNSS Service) das 72 horas anteriores à época de início da previsão. As RNA treinadas foram utilizadas para prever o VTEC por 72 horas (VTEC RNA). Os VTEC RNA foram comparados com os VTEC contidos nos GIM (VTEC GIM). A raiz do erro médio quadrático (RMS) da diferença entre o VTEC GIM e o VTEC RNA variou de 1,4 a 10,7 unidades de TEC (TECU). O erro relativo mostra que a RNA proposta foi capaz de prever o VTEC com 70 a 85% de acerto
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