Signaling Overhead has always been a concern for network operators. LTE offers many improvements aimed at improved network performance and management. This thesis exploit Tracking Area List (TAL) concept in LTE networks. An algorithm to design TAL using UE traces is developed. The performance of TAL design is compared to conventional TA design. Performance is also compared with rule of thumb TAL design which is another approach to designing TAL

In this thesis we directly consider an object tracking problem for wireless sensor networks (WSNs), called track persistence. Track persistence temporally extends the problem of object tracking by seeking to store and retrieve the entire history of an object. To provide an initial solution to track persistence, we develop two distinct algorithms. The first algorithm, update to sink, translates track persistence into a centralized problem. The second algorithm, a linked list-like algorithm, builds a dynamic data structure as the object traverses the network, and rebuilds the object history distributively upon demand. We conduct worst case analysis upon both of these algorithms. Finally, we implement a simulation environment and run a number of tests upon both algorithms. Track persistence is a very challenging problem, and this thesis contributes a pair of solutions which stand as a basis for future research. / Thesis (Master, Computing) -- Queen's University, 2010-09-09 12:56:50.921

Die Kombination von Eyetracking und fMRI in den Neurowissenschaften ist eine relativ neue Methode, die einerseits eine technische Herauforderung darstellt, andererseits neue Möglichkeiten des Zugangs zu neuronalen Prozessen darbietet. In der vorliegenden Arbeit wurden durch Kombination beider Methoden Prozesse der neuronalen und visuellen Verarbeitung von Emotionen untersucht. Zunächst wurde die Rolle von verschiedenen Gehirnregionen innerhalb des emotionalen Netzwerks sowie die Frage nach der Lateralität der emotionalen Verarbeitung untersucht. Die Ergebnisse zeigten, dass die neuronale Antwort in den unterschiedlichen Regionen in erster Linie die Anforderungen an die jeweilige funktionelle Einheit spiegelt. Im Rahmen der Untersuchungen von visueller Verarbeitung wurden die einzelnen spezifischen Blickbewegungsmuster für Emotionen Angst, Ekel und Freude erstmals charakterisiert. Es wurden auch Habituationseffekte auf die beschriebenen Blickbewegungsmuster untersucht. Die gemeinsame Analyse beider Datensätze zeigte, dass zwischen visuellen und neuronalen Prozessen eine enge qualitative Interaktion besteht. Es wurde ein Zusammenhang zwischen der Betrachtungsdauer und der tiefe der Verarbeitung nachgewiesen.

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This thesis presents a framework for a hybrid model-free marker-less inertial-visual camera pose tracking with an integrated sensor fusion mechanism. The proposed solution addresses the fundamental problem of pose recovery in computer vision and robotics and provides an improved solution for wide-area pose tracking that can be used on mobile platforms and in real-time applications. In order to arrive at a suitable pose tracking algorithm, an in-depth investigation was conducted into current methods and sensors used for pose tracking. Preliminary experiments were then carried out on hybrid GPS-Visual as well as wireless micro-location tracking in order to evaluate their suitability for camera tracking in wide-area or GPS-denied environments. As a result of this investigation a combination of an inertial measurement unit and a camera was chosen as the primary sensory inputs for a hybrid camera tracking system. After following a thorough modelling and mathematical formulation process, a novel and improved hybrid tracking framework was designed, developed and evaluated. The resulting system incorporates an inertial system, a vision-based system and a recursive particle filtering-based stochastic data fusion and state estimation algorithm. The core of the algorithm is a state-space model for motion kinematics which, combined with the principles of multi-view camera geometry and the properties of optical flow and focus of expansion, form the main components of the proposed framework. The proposed solution incorporates a monitoring system, which decides on the best method of tracking at any given time based on the reliability of the fresh vision data provided by the vision-based system, and automatically switches between visual and inertial tracking as and when necessary. The system also includes a novel and effective self-adjusting mechanism, which detects when the newly captured sensory data can be reliably used to correct the past pose estimates. The corrected state is then propagated through to the current time in order to prevent sudden pose estimation errors manifesting as a permanent drift in the tracking output. Following the design stage, the complete system was fully developed and then evaluated using both synthetic and real data. The outcome shows an improved performance compared to existing techniques, such as PTAM and SLAM. The low computational cost of the algorithm enables its application on mobile devices, while the integrated self-monitoring, self-adjusting mechanisms allow for its potential use in wide-area tracking applications.

ITC/USA 2006 Conference Proceedings / The Forty-Second Annual International Telemetering Conference and Technical Exhibition / October 23-26, 2006 / Town and Country Resort & Convention Center, San Diego, California / Recent Constraints on the use of L and S band spectrum led to the search for additional Frequency Domain Bandwidth augmentation for test range telemetry needs. The ITU (International Telecommunications Union) approved X band region is listed as 7000 MHz to 8500 MHz for telemetry space applications. Bandwidth is available within this domain subject to the WARC (World Administrative Radio Consortium) approvals. This paper describes tests and presents results illustrating methodology that is available, and which can be used for conversion of S-band assets to the X band spectral region.

The aim of this thesis is to provide methods for 2D segmentation and 2D/3D tracking, that are both fast and robust to imperfect image information, as caused for example by occlusions, motion blur and cluttered background. We do this by combining high level shape information with simultaneous segmentation and tracking. We base our work on the assumption that the space of possible 2D object shapes can be either generated by projecting down known rigid 3D shapes or learned from 2D shape examples. We minimise the discrimination between statistical foreground and background appearance models with respect to the parameters governing the shape generative process (the 6 degree-of-freedom 3D pose of the 3D shape or the parameters of the learned space). The foreground region is delineated by the zero level set of a signed distance function, and we define an energy over this region and its immediate background surroundings based on pixel-wise posterior membership probabilities. We obtain the differentials of this energy with respect to the parameters governing shape and conduct searches for the correct shape using standard non-linear minimisation techniques. This methodology first leads to a novel rigid 3D object tracker. For a known 3D shape, our optimisation here aims to find the 3D pose that leads to the 2D projection that best segments a given image. We extend our approach to track multiple objects from multiple views and propose novel enhancements at the pixel level based on temporal consistency. Finally, owing to the per pixel nature of much of the algorithm, we support our theoretical approach with a real-time GPU based implementation. We next use our rigid 3D tracker in two applications: (i) a driver assistance system, where the tracker is augmented with 2D traffic sign detections, which, unlike previous work, allows for the relevance of the traffic signs to the driver to be gauged and (ii) a robust, real time 3D hand tracker that uses data from an off-the-shelf accelerometer and articulated pose classification results from a multiclass SVM classifier. Finally, we explore deformable 2D/3D object tracking. Unlike previous works, we use a non-linear and probabilistic dimensionality reduction, called Gaussian Process Latent Variable Models, to learn spaces of shape. Segmentation becomes a minimisation of an image-driven energy function in the learned space. We can represent both 2D and 3D shapes which we compress with Fourier-based transforms, to keep inference tractable. We extend this method by learning joint shape-parameter spaces, which, novel to the literature, enable simultaneous segmentation and generic parameter recovery. These can describe anything from 3D articulated pose to eye gaze. We also propose two novel extensions to standard GP-LVM: a method to explore the multimodality in the joint space efficiently, by learning a mapping from the latent space to a space that encodes the similarity between shapes and a method for obtaining faster convergence and greater accuracy by use of a hierarchy of latent embeddings.

In biology, many different kinds of microscopy are used to study cells. There are many different kinds of transmission microscopy, where light is passed through the cells, that can be used without staining or other treatments that can harm the cells. There is also fluorescence microscopy, where fluorescent proteins or dyes are placed in the cells or in parts of the cells, so that they emit light of a specific wavelength when they are illuminated with light of a different wavelength. Many fluorescence microscopes can take images on many different depths in a sample and thereby build a three-dimensional image of the sample. Fluorescence microscopy can also be used to study particles, for example viruses, inside cells. Modern microscopes often have digital cameras or other equipment to take images or record time-lapse video. When biologists perform experiments on cells, they often record image sequences or sequences of three-dimensional volumes to see how the cells behave when they are subjected to different drugs, culture substrates, or other external factors. Previously, the analysis of recorded data has often been done manually, but that is very time-consuming and the results often become subjective and hard to reproduce. Therefore there is a great need for technology for automated analysis of image sequences with cells and particles inside cells. Such technology is needed especially in biological research and drug development. But the technology could also be used clinically, for example to tailor a cancer treatment to an individual patient by evaluating different treatments on cells from a biopsy. This thesis presents algorithms to find cells and particles in images, and to calculate tracks that show how they have moved during an experiment. We have developed a complete system that can find and track cells in all commonly used imaging modalities. We selected and extended a number of existing segmentation algorithms, and thereby created a complete tool to find cell outlines. To link the segmented objects into tracks, we developed a new track linking algorithm. The algorithm adds tracks one by one using dynamic programming, and has many advantages over prior algorithms. Among other things, it is fast, it calculates tracks which are optimal for the entire image sequence, and it can handle situations where multiple cells have been segmented incorrectly as one object. To make it possible to use information about the velocities of the objects in the linking, we developed a method where the positions of the objects are preprocessed using a filter before the linking is performed. This is important for tracking of some particles inside cells and for tracking of cell nuclei in some embryos.       We have developed an open source software which contains all tools that are necessary to analyze image sequences with cells or particles. It has tools for segmentation and tracking of objects, optimization of settings, manual correction, and analysis of outlines and tracks. We developed the software together with biologists who used it in their research. The software has already been used for data analysis in a number of biology publications. Our system has also achieved outstanding performance in three international objective comparisons of systems for tracking of cells. / Inom biologi används många olika typer av mikroskopi för att studera celler. Det finns många typer av genomlysningsmikroskopi, där ljus passerar genom cellerna, som kan användas utan färgning eller andra åtgärder som riskerar att skada cellerna. Det finns också fluorescensmikroskopi där fluorescerande proteiner eller färger förs in i cellerna eller i delar av cellerna, så att de emitterar ljus av en viss våglängd då de belyses med ljus av en annan våglängd. Många fluorescensmikroskop kan ta bilder på flera olika djup i ett prov och på så sätt bygga upp en tre-dimensionell bild av provet. Fluorescensmikroskopi kan även användas för att studera partiklar, som exempelvis virus, inuti celler. Moderna mikroskop har ofta digitala kameror eller liknande utrustning för att ta bilder och spela in bildsekvenser. När biologer gör experiment på celler spelar de ofta in bildsekvenser eller sekvenser av tre-dimensionella volymer för att se hur cellerna beter sig när de utsätts för olika läkemedel, odlingssubstrat, eller andra yttre faktorer. Tidigare har analysen av inspelad data ofta gjorts manuellt, men detta är mycket tidskrävande och resultaten blir ofta subjektiva och svåra att reproducera. Därför finns det ett stort behov av teknik för automatiserad analys av bildsekvenser med celler och partiklar inuti celler. Sådan teknik behövs framförallt inom biologisk forskning och utveckling av läkemedel. Men tekniken skulle också kunna användas kliniskt, exempelvis för att skräddarsy en cancerbehandling till en enskild patient genom att utvärdera olika behandlingar på celler från en biopsi. I denna avhandling presenteras algoritmer för att hitta celler och partiklar i bilder, och för att beräkna trajektorier som visar hur de har förflyttat sig under ett experiment. Vi har utvecklat ett komplett system som kan hitta och följa celler i alla vanligt förekommande typer av mikroskopi. Vi valde ut och vidareutvecklade ett antal existerande segmenteringsalgoritmer, och skapade på så sätt ett heltäckande verktyg för att hitta cellkonturer. För att länka ihop de segmenterade objekten till trajektorier utvecklade vi en ny länkningsalgoritm. Algoritmen lägger till trajektorier en och en med hjälp av dynamisk programmering, och har många fördelar jämfört med tidigare algoritmer. Bland annat är den snabb, den beräknar trajektorier som är optimala över hela bildsekvensen, och den kan hantera fall då flera celler felaktigt segmenterats som ett objekt. För att kunna använda information om objektens hastighet vid länkningen utvecklade vi en metod där objektens positioner förbehandlas med hjälp av ett filter innan länkningen utförs. Detta är betydelsefullt för följning av vissa partiklar inuti celler och för följning av cellkärnor i vissa embryon. Vi har utvecklat en mjukvara med öppen källkod, som innehåller alla verktyg som krävs för att analysera bildsekvenser med celler eller partiklar. Den har verktyg för segmentering och följning av objekt, optimering av inställningar, manuell korrektion, och analys av konturer och trajektorier. Vi utvecklade mjukvaran i samarbete med biologer som använde den i sin forskning. Mjukvaran har redan använts för dataanalys i ett antal biologiska publikationer. Vårt system har även uppnått enastående resultat i tre internationella objektiva jämförelser av system för följning av celler. / <p>QC 20161125</p>