51 research outputs found

    Forced Migration, the Other Way Round? The Politics of Deporting Afghans from Germany

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    Biochemical, biophysical, and functional characterization of bacterially expressed and refolded receptor binding domain of Plasmodium vivax duffy-binding

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    Invasion of erythrocytes by malaria parasites is mediated by specific molecular interactions. Plasmodium vivax is completely dependent on interaction with the Duffy blood group antigen to invade human erythrocytes. The P. vivax Duffy-binding protein, which binds the Duffy antigen during invasion, belongs to a family of erythrocyte-binding proteins that also includesPlasmodium falciparum sialic acid binding protein andPlasmodium knowlesi Duffy binding protein. The receptor binding domains of these proteins lie in a conserved, N-terminal, cysteine-rich region, region II, found in each of these proteins. Here, we have expressed P. vivax region II (PvRII), the P. vivax Duffy binding domain, in Escherichia coli. Recombinant PvRII is incorrectly folded and accumulates in inclusion bodies. We have developed methods to refold and purify recombinant PvRII in its functional conformation. Biochemical, biophysical, and functional characterization confirms that recombinant PvRII is pure, homogeneous, and functionally active in that it binds Duffy-positive human erythrocytes with specificity. Refolded PvRII is highly immunogenic and elicits high titer antibodies that can inhibit binding of P. vivax Duffy-binding protein to erythrocytes, providing support for its development as a vaccine candidate forP. vivax malaria. Development of methods to produce functionally active recombinant PvRII is an important step for structural studies as well as vaccine development

    Fuzzy Distance Measure Based Affinity Propagation Clustering

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    Affinity Propagation (AP) is an effective algorithm that find exemplars repeatedly exchange real valued messages between pairs of data points. AP uses the similarity between data points to calculate the messages. Hence, the construction of similarity is essential in the AP algorithm. A common choice for similarity is the negative Euclidean distance. However, due to the simplicity of Euclidean distance, it cannot capture the real structure of data. Furthermore, Euclidean distance is sensitive to noise and outliers such that the performance of the AP might be degraded. Therefore, researchers have intended to utilize different similarity measures to analyse the performance of AP. nonetheless, there is still a room to enhance the performance of AP clustering. A clustering method called fuzzy based Affinity propagation (F-AP) is proposed, which is based on a fuzzy similarity measure. Experiments shows the efficiency of the proposed F-AP, experiments is performed on UCI dataset. Results shows a promising improvement on AP

    State-Of-The-Art In Image Clustering Based On Affinity Propagation

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    Proclivity spread (AP) is a productive unsupervised grouping technique, which display a quick execution speed and discover bunches in a low mistake rate. AP calculation takes as info a similitude network that comprise of genuine esteemed likenesses between information focuses. The strategy iteratively trades genuine esteemed messages between sets of information focuses until a decent arrangement of models developed. The development of the comparability network dependent on the Euclidean separation is a significant stage during the time spent AP. Appropriately, the conventional Euclidean separation which is the summation of the pixel-wise force contrasts perform beneath normal when connected for picture grouping, as it endures of being reasonable to exceptions and even to little misshapening in pictures. Studies should be done on different methodologies from existing investigations especially in the field of picture grouping with different datasets. In this way, a sensible picture closeness metric will be researched to suite with datasets in the picture clustering field. As an end, changing the comparability lattice will prompt a superior clustering results

    DBGC:Dimension-Based Generic Convolution Block for Object Recognition

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    The object recognition concept is being widely used a result of increasing CCTV surveillance and the need for automatic object or activity detection from images or video. Increases in the use of various sensor networks have also raised the need of lightweight process frameworks. Much research has been carried out in this area, but the research scope is colossal as it deals with open-ended problems such as being able to achieve high accuracy in little time using lightweight process frameworks. Convolution Neural Networks and their variants are widely used in various computer vision activities, but most of the architectures of CNN are application-specific. There is always a need for generic architectures with better performance. This paper introduces the Dimension-Based Generic Convolution Block (DBGC), which can be used with any CNN to make the architecture generic and provide a dimension-wise selection of various height, width, and depth kernels. This single unit which uses the separable convolution concept provides multiple combinations using various dimension-based kernels. This single unit can be used for height-based, width-based, or depth-based dimensions; the same unit can even be used for height and width, width and depth, and depth and height dimensions. It can also be used for combinations involving all three dimensions of height, width, and depth. The main novelty of DBGC lies in the dimension selector block included in the proposed architecture. Proposed unoptimized kernel dimensions reduce FLOPs by around one third and also reduce the accuracy by around one half; semi-optimized kernel dimensions yield almost the same or higher accuracy with half the FLOPs of the original architecture, while optimized kernel dimensions provide 5 to 6% higher accuracy with around a 10 M reduction in FLOPs

    Advancing sepsis clinical research: harnessing transcriptomics for an omics-based strategy - a comprehensive scoping review

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    Sepsis continues to be recognized as a significant global health challenge across all ages and is characterized by a complex pathophysiology. In this scoping review, PRISMA-ScR guidelines were adhered to, and a transcriptomic methodology was adopted, with the protocol registered on the Open Science Framework. We hypothesized that gene expression analysis could provide a foundation for establishing a clinical research framework for sepsis. A comprehensive search of the PubMed database was conducted with a particular focus on original research and systematic reviews of transcriptomic sepsis studies published between 2012 and 2022. Both coding and non-coding gene expression studies have been included in this review. An effort was made to enhance the understanding of sepsis at the mRNA gene expression level by applying a systems biology approach through transcriptomic analysis. Seven crucial components related to sepsis research were addressed in this study: endotyping (n = 64), biomarker (n = 409), definition (n = 0), diagnosis (n = 1098), progression (n = 124), severity (n = 451), and benchmark (n = 62). These components were classified into two groups, with one focusing on Biomarkers and Endotypes and the other oriented towards clinical aspects. Our review of the selected studies revealed a compelling association between gene transcripts and clinical sepsis, reinforcing the proposed research framework. Nevertheless, challenges have arisen from the lack of consensus in the sepsis terminology employed in research studies and the absence of a comprehensive definition of sepsis. There is a gap in the alignment between the notion of sepsis as a clinical phenomenon and that of laboratory indicators. It is potentially responsible for the variable number of patients within each category. Ideally, future studies should incorporate a transcriptomic perspective. The integration of transcriptomic data with clinical endpoints holds significant potential for advancing sepsis research, facilitating a consensus-driven approach, and enabling the precision management of sepsis
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