397 research outputs found

    Interactive sensor planning

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    This paper describes an interactive sensor planning system, that can be used to select viewpoints subject to camera visibility, field of view and task constraints. Application areas for this method include surveillance planning, safety monitoring, architectural site design planning, and automated site modeling. Given a description, of the sensor's characteristics, the objects in the 3-D scene, and the targets to be viewed, our algorithms compute the set of admissible view points that satisfy the constraints. The system first builds topologically correct solid models of the scene from a variety of data sources. Viewing targets are then selected, and visibility volumes and field of view cones are computed and intersected to create viewing volumes where cameras can be placed. The user can interactively manipulate the scene and select multiple target features to be viewed by a camera. The user can also select candidate viewpoints within this volume to synthesize views and verify the correctness of the planning system. We present experimental results for the planning system on an actual complex city model

    Integration of range and image sensing for photorealistic 3D modeling

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    The automated extraction of photorealistic 3-D models of the world that can be used in applications such as virtual reality, tele-presence, digital cinematography and urban planning, is the focus of this paper. The combination of range (dense depth estimates) and image sensing (color information) provides data-sets which allow us to create photorealistic models of high quality. The challenges are the simplification of the 3-D data set, the extraction of meaningful features in both the range and 2-D images and the fusion of those data-sets using the extracted features. We address all these challenges and provide results on data we gathered in outdoor scenes by a range and image sensor based on a mobile robot. Our ultimate goal is an autonomous 3-D model creation system which minimizes the amount of human interaction

    3-D model construction using range and image data

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    This paper deals with the automated creation of geometric and photometric correct 3-D models of the world. Those models can be used for virtual reality, tele-presence, digital cinematography and urban planning applications. The combination of range (dense depth estimates) and image sensing (color information) provides data-sets which allow us to create geometrically correct, photorealistic models of high quality. The 3-D models are first built from range data using a volumetric set intersection method previously developed by us. Photometry can be mapped onto these models by registering features from both the 3-D and 2-D data sets. Range data segmentation algorithms have been developed to identify planar regions, determine linear features from planar intersections that can serve as features for registration with 2-D imagery lines, and reduce the overall complexity of the models. Results are shown for building models of large buildings on our campus using real data acquired from multiple sensors

    Automated model acquisition from range images with view planning

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    We present an incremental system that builds accurate CAD models of objects from multiple range images. Using a hybrid of surface mesh and volumetric representations, the system creates a "water-tight" 3D model at each step of the modeling process, allowing reasonable models to be built from a small number of views. We also present a method that can be used to plan the next view and reduce the number of scans needed to recover the object. Results are presented for the creation of 3D models of a computer game controller, a hip joint prosthesis, and a mechanical strut

    3-D modeling from range imagery: an incremental method with a planning component

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    In this paper we present a method for automatically constructing a CAD model of an unknown object from range images. The method is an incremental one that interleaves a sensing operation that acquires and merges information into the model with a planning phase to determine the next sensor position or "view". This is accomplished by integrating a system for 3-D model acquisition with a sensor planner. The model acquisition system provides facilities for range image acquisition, solid model construction and model merging: both mesh surface and solid representations are used to build a model of the range data from each view, which is then merged with the model built from previous sensing operations. The planning system utilizes the resulting incomplete model to plan the next sensing operation by finding a sensor viewpoint that will improve the fidelity of the model. Experimental results are presented for a complex part that includes polygonal faces, curved surfaces, and large self-occlusions

    β-Catenin is a pH sensor with decreased stability at higher intracellular pH.

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    β-Catenin functions as an adherens junction protein for cell-cell adhesion and as a signaling protein. β-catenin function is dependent on its stability, which is regulated by protein-protein interactions that stabilize β-catenin or target it for proteasome-mediated degradation. In this study, we show that β-catenin stability is regulated by intracellular pH (pHi) dynamics, with decreased stability at higher pHi in both mammalian cells and Drosophila melanogaster β-Catenin degradation requires phosphorylation of N-terminal residues for recognition by the E3 ligase β-TrCP. While β-catenin phosphorylation was pH independent, higher pHi induced increased β-TrCP binding and decreased β-catenin stability. An evolutionarily conserved histidine in β-catenin (found in the β-TrCP DSGIHS destruction motif) is required for pH-dependent binding to β-TrCP. Expressing a cancer-associated H36R-β-catenin mutant in the Drosophila eye was sufficient to induce Wnt signaling and produced pronounced tumors not seen with other oncogenic β-catenin alleles. We identify pHi dynamics as a previously unrecognized regulator of β-catenin stability, functioning in coincidence with phosphorylation

    Laws of biology: why so few?

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    Finding fundamental organizing principles is the current intellectual front end of systems biology. From a hydrogen atom to the whole cell level, organisms manage massively parallel and massively interactive processes over several orders of magnitude of size. To manage this scale of informational complexity it is natural to expect organizing principles that determine higher order behavior. Currently, there are only hints of such organizing principles but no absolute evidences. Here, we present an approach as old as Mendel that could help uncover fundamental organizing principles in biology. Our approach essentially consists of identifying constants at various levels and weaving them into a hierarchical chassis. As we identify and organize constants, from pair-wise interactions to networks, our understanding of the fundamental principles in biology will improve, leading to a theory in biology

    Loss of Adenomatous polyposis coli function renders intestinal epithelial cells resistant to the cytokine IL-22

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    Interleukin-22 (IL-22) is a critical immune defence cytokine that maintains intestinal homeostasis and promotes wound healing and tissue regeneration, which can support the growth of colorectal tumours. Mutations in the adenomatous polyposis coli gene (Apc) are a major driver of familial colorectal cancers (CRCs). How IL-22 contributes to APC-mediated tumorigenesis is poorly understood. To investigate IL-22 signalling in wild-type (WT) and APC-mutant cells, we performed RNA sequencing (RNAseq) of IL-22-treated murine small intestinal epithelial organoids. In WT epithelia, antimicrobial defence and cellular stress response pathways were most strongly induced by IL-22. Surprisingly, although IL-22 activates signal transducer and activator of transcription 3 (STAT3) in APC-mutant cells, STAT3 target genes were not induced. Our analyses revealed that ApcMin/Min cells are resistant to IL-22 due to reduced expression of the IL-22 receptor, and increased expression of inhibitors of STAT3, particularly histone deacetylases (HDACs). We further show that IL-22 increases DNA damage and genomic instability, which can accelerate cellular transition from heterozygosity (ApcMin/+) to homozygosity (ApcMin/Min) to drive tumour formation. Our data reveal an unexpected role for IL-22 in promoting early tumorigenesis while excluding a function for IL-22 in transformed epithelial cells
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