135 research outputs found

    Capacity Analysis for Continuous Alphabet Channels with Side Information, Part I: A General Framework

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    Capacity analysis for channels with side information at the receiver has been an active area of interest. This problem is well investigated for the case of finite alphabet channels. However, the results are not easily generalizable to the case of continuous alphabet channels due to analytic difficulties inherent with continuous alphabets. In the first part of this two-part paper, we address an analytical framework for capacity analysis of continuous alphabet channels with side information at the receiver. For this purpose, we establish novel necessary and sufficient conditions for weak* continuity and strict concavity of the mutual information. These conditions are used in investigating the existence and uniqueness of the capacity-achieving measures. Furthermore, we derive necessary and sufficient conditions that characterize the capacity value and the capacity-achieving measure for continuous alphabet channels with side information at the receiver.Comment: Submitted to IEEE Trans. Inform. Theor

    A method of color filter array interpolation with alias cancellation properties

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    ABSTRACT Digital still cameras use a single charge-coupled device (CCD) sensor array and a color filter array (CFA) to sample a full-color image. Thus, the measured image is an interleaving of the subsampled red, green, and blue images. The red and blue images are sampled at a lower rate, so if standard interpolation techniques are used, the reconstructed red and blue images will be missing some highfrequency information and could contain distortions from aliasing. This paper proposes a method of CFA interpolation that combines information from the green image with the subsampled red and blue images to attack these problems. The green high-frequency information is added to the interpolated red and blue images to increase the sharpness of the output and is also used to estimate the aliasing in the interpolated red and blue images, providing a means of reducing the appearance of the aliasing distortions

    Image-based photo hulls for fast and photo-realistic new view synthesis

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    We present an efficient image-based rendering algorithm that generates views of a scene's photo hull. The photo hull is the largest 3D shape that is photo-consistent with photographs taken of the scene from multiple viewpoints. Our algorithm, image-based photo hulls (IBPH), like the image-based visual hulls (IBVH) algorithm from Matusik et al. on which it is based, takes advantage of epipolar geometry to efficiently reconstruct the geometry and visibility of a scene. Our IBPH algorithm differs from IBVH in that it utilizes the color information of the images to identify scene geometry. These additional color constraints result in more accurately reconstructed geometry, which often projects to better synthesized virtual views of the scene. We demonstrate our algorithm running in a realtime 3D telepresence application using video data acquired from multiple viewpoints

    Probing the Early Stages of Low-Mass Star Formation in LDN 1689N: Dust and Water in IRAS 16293-2422A, B, and E

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    We present deep images of dust continuum emission at 450, 800, and 850 micron of the dark cloud LDN 1689N which harbors the low-mass young stellar objects (YSOs) IRAS 16293-2422A and B (I16293A and I16293B) and the cold prestellar object I16293E. Toward the positions of I16293A and E we also obtained spectra of CO-isotopomers and deep submillimeter observations of chemically related molecules with high critical densities. To I16293A we report the detection of the HDO 1_01 - 0_00 and H2O 1_10 - 1_01 ground-state transitions as broad self-reversed emission profiles with narrow absorption, and a tentative detection of H2D+ 1_10 - 1_11. To I16293E we detect weak emission of subthermally excited HDO 1_01 - 0_00. Based on this set of submillimeter continuum and line data we model the envelopes around I16293A and E. The density and velocity structure of I16293A is fit by an inside-out collapse model, yielding a sound speed of a=0.7 km/s, an age of t=(0.6--2.5)e4 yr, and a mass of 6.1 Msun. The density in the envelope of I16293E is fit by a radial power law with index -1.0+/-0.2, a mass of 4.4 Msun, and a constant temperature of 16K. These respective models are used to study the chemistry of the envelopes of these pre- and protostellar objects. The [HDO]/[H2O] abundance ratio in the warm inner envelope of I16293A of a few times 1e-4 is comparable to that measured in comets. This supports the idea that the [HDO]/[H2O] ratio is determined in the cold prestellar core phase and conserved throughout the formation process of low-mass stars and planets.Comment: 61 pages, 17 figures. Accepted for publication in ApJ. To get Fig. 13: send email to [email protected]

    Characterization of Engineered Actin Binding Proteins That Control Filament Assembly and Structure

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    Eukaryotic cells strictly regulate the structure and assembly of their actin filament networks in response to various stimuli. The actin binding proteins that control filament assembly are therefore attractive targets for those who wish to reorganize actin filaments and reengineer the cytoskeleton. Unfortunately, the naturally occurring actin binding proteins include only a limited set of pointed-end cappers, or proteins that will block polymerization from the slow-growing end of actin filaments. Of the few that are known, most are part of large multimeric complexes that are challenging to manipulate.We describe here the use of phage display mutagenesis to generate of a new class of binding protein that can be targeted to the pointed-end of actin. These proteins, called synthetic antigen binders (sABs), are based on an antibody-like scaffold where sequence diversity is introduced into the binding loops using a novel "reduced genetic code" phage display library. We describe effective strategies to select and screen for sABs that ensure the generated sABs bind to the pointed-end surface of actin exclusively.From our set of pointed-end binders, we identify three sABs with particularly useful properties to systematically probe actin dynamics: one protein that caps the pointed end, a second that crosslinks actin filaments, and a third that severs actin filaments and promotes disassembly

    Research Reports Andean Past 6

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    In Support of a Patient-Driven Initiative and Petition to Lower the High Price of Cancer Drugs

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    Comment in Lowering the High Cost of Cancer Drugs--III. [Mayo Clin Proc. 2016] Lowering the High Cost of Cancer Drugs--I. [Mayo Clin Proc. 2016] Lowering the High Cost of Cancer Drugs--IV. [Mayo Clin Proc. 2016] In Reply--Lowering the High Cost of Cancer Drugs. [Mayo Clin Proc. 2016] US oncologists call for government regulation to curb drug price rises. [BMJ. 2015

    52 Genetic Loci Influencing Myocardial Mass.

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    BACKGROUND: Myocardial mass is a key determinant of cardiac muscle function and hypertrophy. Myocardial depolarization leading to cardiac muscle contraction is reflected by the amplitude and duration of the QRS complex on the electrocardiogram (ECG). Abnormal QRS amplitude or duration reflect changes in myocardial mass and conduction, and are associated with increased risk of heart failure and death. OBJECTIVES: This meta-analysis sought to gain insights into the genetic determinants of myocardial mass. METHODS: We carried out a genome-wide association meta-analysis of 4 QRS traits in up to 73,518 individuals of European ancestry, followed by extensive biological and functional assessment. RESULTS: We identified 52 genomic loci, of which 32 are novel, that are reliably associated with 1 or more QRS phenotypes at p < 1 × 10(-8). These loci are enriched in regions of open chromatin, histone modifications, and transcription factor binding, suggesting that they represent regions of the genome that are actively transcribed in the human heart. Pathway analyses provided evidence that these loci play a role in cardiac hypertrophy. We further highlighted 67 candidate genes at the identified loci that are preferentially expressed in cardiac tissue and associated with cardiac abnormalities in Drosophila melanogaster and Mus musculus. We validated the regulatory function of a novel variant in the SCN5A/SCN10A locus in vitro and in vivo. CONCLUSIONS: Taken together, our findings provide new insights into genes and biological pathways controlling myocardial mass and may help identify novel therapeutic targets
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