909 resultados para Chipless RFID tag


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In this paper we present a novel Radio Frequency Identification (RFID) system for accurate indoor localization. The system is composed of a standard Ultra High Frequency (UHF), ISO-18006C compliant RFID reader, a large set of standard passive RFID tags whose locations are known, and a newly developed tag-like RFID component that is attached to the items that need to be localized. The new semi-passive component, referred to as sensatag (sense-a-tag), has a dual functionality wherein it can sense the communication between the reader and standard tags which are in its proximity, and also communicate with the reader like standard tags using backscatter modulation. Based on the information conveyed by the sensatags to the reader, localization algorithms based on binary sensor principles can be developed. We present results from real measurements that show the accuracy of the proposed system.

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Este trabajo presenta un sistema de posicionamiento local (LPS) para personas en entornos interiores basado en la combinación de tecnología RFID activa y una metodología bayesiana de estimación de la posición a partir de la fuerza de las señales de RF recibidas. La complejidad inherente a la propagación de las ondas de RF en entornos interiores causa grandes fluctuaciones en el nivel de la fuerza de la señal, por lo que las técnicas bayesianas, de naturaleza estadística, tienen ventajas significativas frente a métodos de posicionamiento más comunes, como multilateración, minimización cuadrática o localización por fingerprinting. En la validación experimental del sistema RFID-LPS se consigue un error de posicionamiento medio de 2.10 m (mediana de 1.84 m y 3.89 m en el 90% de los casos), en un área abarcada de 475 m2 con 29 tags RFID, y con velocidades de desplazamiento de hasta 0.5 m/s, prestaciones iguales o superiores a otros sistemas del estado del arte. Aunque existen precedentes en Robótica móvil, la combinación de métodos bayesianos y tecnología RFID activa usada en este trabajo es original en el marco de los sistemas de localización de personas, cuyos desplazamientos son generalmente más impredecibles que los de los robots. Otros aspectos novedosos investigados son la posibilidad de alcanzar una estimación conjunta de posición y orientación de un usuario con dos métodos distintos (uso de antenas directivas y aprovechamiento de la atenuación de la señal de RF por el cuerpo humano), la escalabilidad del sistema RFID-LPS, y la estimación de la posición por técnicas bayesianas en sistemas simples que pueden detectar los marcadores RFID, pero no medir su fuerza de señal.

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La fermentación de las bayas de café se considera una et apa crítica en el procesado del café debido a su impacto en la calidad final del producto. La temperatura es una de las principales variables de control que puede ser utilizada para predecir el final del proceso, teniendo en cuenta que varios autores indican que el control de esta etapa es fundamental para evitar la mala calidad de la be bida final. En la práctica, la fermentación es el paso menos controlado del proceso, haciendo que los beneficiaderos operen lejos de sus condiciones óptimas en términos de costes de operación (es decir, elevados consumos de energía y agua) y de calidad del producto final. El objetivo de este trabajo es caracterizar los gradientes de temperatura que se dan en los tanques de fermentación mediante una red multi-distribuida de sensores autónomos, inalámbricos y de bajo coste (registradores de temperatura del tipo RFID, identificadores de radiofrecuencia semipasivos modelo TurboTag®).Para ello se utilizan dos metodologías: la interpolación espacial en coordenadas polares y los diagramas de espacio de fase. Se supervisaron dos fermentaciones reales de café, en El Cauca (Colombia), mediante sensores sumergidos directamente en la masa en fermentación. Los fermentadores eran tanques de plástico cubiertos, uno de ellos colocado en el interior de un almacén, permaneciendo el otro a la intemperie. El rango de variación máximo de temperatura en los tanques fue de 4,5ºC. La interpolación espacial mostró, incluso en el fermentador bajo las condiciones menos desfavorables en el interior del almacén, un gradiente radial de temperatura instantáneo de 0,1 °C/cm desde el centro hasta el perímetro del tanque y un gradiente vertical de temperatura de 0,25 °C/cm para sensores con coordenadas polares iguales. La combinación de ambas metodologías permitió la identificación consistente de los puntos calientes y fríos de ambas fermentaciones.

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Las hortalizas mínimamente procesadas (MP) son productos frescos, higienizados, que sufren alteraciones físicas durante el proceso de elaboración que afectan a su metabolismo, determinando incrementos en la tasa respiratoria y producción de etileno. Los daños que se originan por las operaciones físicas, vuelven a estos productos más susceptibles a la colonización de microorganismos, inducen procesos de cicatrización de heridas y afectan su calidad organoléptica y funcional. Por ello en estos productos es especialmente crítico el aseguramiento de las condiciones de refrigeración desde el productor hasta el consumidor. En este estudio se presenta el análisis de las temperaturas registradas en Santiago (Chile) durante la cadena de producción y distribución de lechugas baby leaf MP tipo Salanova®, monitorizadas mediante sensores de temperatura y humedad relativa (I-Buttons®) y tarjetas RFID con sensor de temperatura (TurboTag®), colocados en el interior de las bolsas de lechuga y en el exterior de las cajas de agrupación. El objetivo del presente trabajo es generar información sobre el historial térmico de estos productos desde la huerta a la nevera del consumidor, así como optimizar los protocolos de colocación de dispositivos y sistematizar procedimientos de análisis de datos espacio-temporales. Con los datos registrados, se simuló la cadena de producción, distribución y venta, realizando un seguimiento de la calidad comercial del producto, evaluándose la tasa respiratoria y las características sensoriales sin degustación. Se observó que no solo se producen saltos térmicos discretos, sino que las lechugas estuvieron durante gran parte de su vida útil en condiciones sub-óptimas de temperatura, comprometiéndose su calidad sensorial.

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A new technology is being proposed as a solution to the problem of unintentional facial detection and recognition in pictures in which the individuals appearing want to express their privacy preferences, through the use of different tags. The existing methods for face de-identification were mostly ad hoc solutions that only provided an absolute binary solution in a privacy context such as pixelation, or a bar mask. As the number and users of social networks are increasing, our preferences regarding our privacy may become more complex, leaving these absolute binary solutions as something obsolete. The proposed technology overcomes this problem by embedding information in a tag which will be placed close to the face without being disruptive. Through a decoding method the tag will provide the preferences that will be applied to the images in further stages.

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Acknowledgements We thank Andrew Spink (Noldus Information Technology) and the Blogging Birds team members Peter Kindness and Abdul Adeniyi for their valuable contributions to this paper. John Fryxell, Chris Thaxter and Arjun Amar provided valuable comments on an earlier version. The study was part of the Digital Conservation project of dot.rural, the University of Aberdeen’s Digital Economy Research Hub, funded by RCUK (grant reference EP/G066051/1).

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Inclui notas explicativas e bibliografia

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A novel multiple affinity purification (MAFT) or tandem affinity purification (TAP) tag has been constructed. It consists of the calmodulin binding peptide, six histidine residues, and three copies of the hemagglutinin epitope. This ‘CHH’ MAFT tag allows two or three consecutive purification steps, giving high purity. Active Clb2–Cdc28 kinase complex was purified from yeast cells after inserting the CHH tag into Clb2. Associated proteins were identified using mass spectrometry. These included the known associated proteins Cdc28, Sic1 and Cks1. Several other proteins were found including the 70 kDa chaperone, Ssa1.

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Expressed sequence tags (ESTs) are randomly sequenced cDNA clones. Currently, nearly 3 million human and 2 million mouse ESTs provide valuable resources that enable researchers to investigate the products of gene expression. The EST databases have proven to be useful tools for detecting homologous genes, for exon mapping, revealing differential splicing, etc. With the increasing availability of large amounts of poorly characterised eukaryotic (notably human) genomic sequence, ESTs have now become a vital tool for gene identification, sometimes yielding the only unambiguous evidence for the existence of a gene expression product. However, BLAST-based Web servers available to the general user have not kept pace with these developments and do not provide appropriate tools for querying EST databases with large highly spliced genes, often spanning 50 000–100 000 bases or more. Here we describe Gene2EST (http://woody.embl-heidelberg.de/gene2est/), a server that brings together a set of tools enabling efficient retrieval of ESTs matching large DNA queries and their subsequent analysis. RepeatMasker is used to mask dispersed repetitive sequences (such as Alu elements) in the query, BLAST2 for searching EST databases and Artemis for graphical display of the findings. Gene2EST combines these components into a Web resource targeted at the researcher who wishes to study one or a few genes to a high level of detail.

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STACK is a tool for detection and visualisation of expressed transcript variation in the context of developmental and pathological states. The datasystem organises and reconstructs human transcripts from available public data in the context of expression state. The expression state of a transcript can include developmental state, pathological association, site of expression and isoform of expressed transcript. STACK consensus transcripts are reconstructed from clusters that capture and reflect the growing evidence of transcript diversity. The comprehensive capture of transcript variants is achieved by the use of a novel clustering approach that is tolerant of sub-sequence diversity and does not rely on pairwise alignment. This is in contrast with other gene indexing projects. STACK is generated at least four times a year and represents the exhaustive processing of all publicly available human EST data extracted from GenBank. This processed information can be explored through 15 tissue-specific categories, a disease-related category and a whole-body index and is accessible via WWW at http://www.sanbi.ac.za/Dbases.html. STACK represents a broadly applicable resource, as it is the only reconstructed transcript database for which the tools for its generation are also broadly available (http://www.sanbi.ac.za/CODES).

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Molecular and fragment ion data of intact 8- to 43-kDa proteins from electrospray Fourier-transform tandem mass spectrometry are matched against the corresponding data in sequence data bases. Extending the sequence tag concept of Mann and Wilm for matching peptides, a partial amino acid sequence in the unknown is first identified from the mass differences of a series of fragment ions, and the mass position of this sequence is defined from molecular weight and the fragment ion masses. For three studied proteins, a single sequence tag retrieved only the correct protein from the data base; a fourth protein required the input of two sequence tags. However, three of the data base proteins differed by having an extra methionine or by missing an acetyl or heme substitution. The positions of these modifications in the protein examined were greatly restricted by the mass differences of its molecular and fragment ions versus those of the data base. To characterize the primary structure of an unknown represented in the data base, this method is fast and specific and does not require prior enzymatic or chemical degradation.

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We applied the directional tag PCR subtractive hybridization method to construct a rat hypothalamic cDNA library from which cerebellar and hippocampal sequences had been depleted, enriching 20-30-fold for sequences expressed selectively in the hypothalamus. We studied a sample of 94 clones selected for enrichment in the subtracted library. These clones corresponded to 43 distinct mRNA species, about half of which were novel. Thirty-eight of these 43 mRNAs (corresponding to 85 of the clones in the sample) exhibited enrichment in the hypothalamus; 23 were highly enriched. In situ hybridization studies revealed that one novel species was restricted to cells in a small bilaterally symmetric area of the paraventricular hypothalamus. Other novel mRNAs showed substantial enrichment in basal diencephalic structures, particularly the hypothalamus, without restriction to single hypothalamic nuclei. The data suggest that the hypothalamus utilizes at least two distinct strategies for employing its selectively expressed proteins. Secretory neuropeptides utilized for intercellular communication are produced by functionally discrete nuclei, while several other proteins are shared by structures that are unrelated in their physiological roles but may share biochemical systems.