378 research outputs found

    Experimental measurements of the RF sheath thickness with a cylindrical Langmuir probe

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    The plasma-wall transition with collisions and an oblique magnetic field: reversal of potential drops at grazing incidences

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    International audienceThe plasma-wall transition is studied by using 1d3V particle-in-cell (PIC) simulations in the case of a one dimensional plasma bounded by two absorbing walls separated by 200 Debye lengths (λ d). A constant and oblique magnetic field is applied to the system, with an amplitude such that r < λ d < R, where r and R are the electron and ion Larmor radius respectively. Collisions with neutrals are taken into account and modelled by an energy conservative operator, which randomly reorients ion and electron velocities. The plasma-wall transition (PWT) is shown to depend on both the angle of incidence of the magnetic field with respect to the wall θ, and on the ion mean-free-path to Larmor radius ratio, λ ci /R. In the very low collisionality regime (λ ci R) and for a large angle of incidence, the PWT consists in the classical tri-layer structure (Debye sheath / Chodura sheath / Pre-sheath) from the wall towards the center of the plasma. The drops of potential within the different regions are well consistent with already published models. However, when sin θ ≤ R/λ ci or with the ordering λ ci < R , collisions can not be neglected, leading to the disappearance of the Chodura sheath. In these case, a collisional model yields analytic expressions for the potential drop in the quasi-neutral region, and explains, in qualitative and quantitative agreement with the simulation results, its reversal below a critical angle derived in the paper, a regime possibly met in the SOL of tokamaks. It is further shown that the potential drop in the Debye sheath slightly varies with the collision-ality for λ ci R. However, it tends to decrease with λ ci in the high collisionality regime, until the Debye sheath finally vanishes

    Characterization of transport of titanium neutral atoms sputtered in Ar and Ar/N 2 HIPIMS discharges

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    International audienceIn this work we report on the investigation of the transport behavior of Ti neutral atoms sputtered in a reactive high power impulse magnetron sputtering device used for TiN coating deposition. The time-resolved tunable diode laser induced fluorescence (TR-TDLIF), previously developed to study the transport of tungsten atoms, was improved to measure Ti neutral atom velocity distribution functions. We find that the TR-TDLIF signal has to be fitted using three Gaussian distributions, corresponding to the energetic, thermalized, and quasi-thermalized (atoms with non-zero mean velocity) atom populations. The ability to distinguish populations of atoms and to determine their corresponding deposited flux and energy may be of great interest to control film properties as desired for targeted applications. From the fitting, the vapor transport parameters (flux and energy) are calculated and studied as a function of distance from the target, pressure, and percentage of nitrogen in an Ar/N2 gas mixture. The study focuses on the effect of added nitrogen on the transport of sputtered atoms

    Experimental and theoretical study of bumped characteristics obtained with cylindrical Langmuir probe in magnetized Helium plasma

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    Cylindrical Langmuir probe measurements in a Helium plasma were performed and analysed in the presence of a magnetic field. The plasma is generated in the ALINE device, a cylindrical vessel 1 m long and 30 cm in diameter using a direct coupled RF antenna (ν RF = 25 MHz). The density and temperature are of the order of 10 16 m −3 and 1.5 eV, respectively, for 1.2 Pa Helium pressure and 200 W RF power. The axial magnetic field can be set from 0 up to 0.1 T, and the plasma diagnostic is a RF compensated Langmuir probe, which can be tilted with respect to the magnetic field lines. In the presence of a magnetic field, I(V) characteristics look like asymmetrical double probe ones (tanh-shape), which is due to the trapping of charged particles inside a flux tube connected to the probe on one side and to the wall on the other side. At low tilting angle, high magnetic field amplitude, power magnitude and low He pressure, which are the parameters scanned in our study, a bump can appear on the I(V) in the plasma potential range. We then compare different models for deducing plasma parameters from such unusual bumped curves. Finally, using a fluid model, the bump rising on the characteristics can be explained, assuming a density depletion in the flux tube, and emphasizing the role of the perpendicular transport of ions

    New Technologies for the Identification of Novel Genetic Markers of Disorders of Sex Development (DSD)

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    Although the genetic basis of human sexual determination and differentiation has advanced considerably in recent years, the fact remains that in most subjects with disorders of sex development (DSD) the underlying genetic cause is unknown. Where pathogenic mutations have been identified, the phenotype can be highly variable, even within families, suggesting that other genetic variants are influencing the expression of the phenotype. This situation is likely to change, as more powerful and affordable tools become widely available for detailed genetic analyses. Here, we describe recent advances in comparative genomic hybridisation, sequencing by hybridisation and next generation sequencing, and we describe how these technologies will have an impact on our understanding of the genetic causes of DSD

    Explainable Anatomical Shape Analysis through Deep Hierarchical Generative Models

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    Quantification of anatomical shape changes currently relies on scalar global indexes which are largely insensitive to regional or asymmetric modifications. Accurate assessment of pathology-driven anatomical remodeling is a crucial step for the diagnosis and treatment of many conditions. Deep learning approaches have recently achieved wide success in the analysis of medical images, but they lack interpretability in the feature extraction and decision processes. In this work, we propose a new interpretable deep learning model for shape analysis. In particular, we exploit deep generative networks to model a population of anatomical segmentations through a hierarchy of conditional latent variables. At the highest level of this hierarchy, a two-dimensional latent space is simultaneously optimised to discriminate distinct clinical conditions, enabling the direct visualisation of the classification space. Moreover, the anatomical variability encoded by this discriminative latent space can be visualised in the segmentation space thanks to the generative properties of the model, making the classification task transparent. This approach yielded high accuracy in the categorisation of healthy and remodelled left ventricles when tested on unseen segmentations from our own multi-centre dataset as well as in an external validation set, and on hippocampi from healthy controls and patients with Alzheimer's disease when tested on ADNI data. More importantly, it enabled the visualisation in three-dimensions of both global and regional anatomical features which better discriminate between the conditions under exam. The proposed approach scales effectively to large populations, facilitating high-throughput analysis of normal anatomy and pathology in large-scale studies of volumetric imaging

    Robust whole-brain segmentation: Application to traumatic brain injury

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    We propose a framework for the robust and fully-automatic segmentation of magnetic resonance (MR) brain images called "Multi-Atlas Label Propagation with Expectation-Maximisation based refinement" (MALP-EM). The presented approach is based on a robust registration approach (MAPER), highly performant label fusion (joint label fusion) and intensity-based label refinement using EM. We further adapt this framework to be applicable for the segmentation of brain images with gross changes in anatomy. We propose to account for consistent registration errors by relaxing anatomical priors obtained by multi-atlas propagation and a weighting scheme to locally combine anatomical atlas priors and intensity-refined posterior probabilities. The method is evaluated on a benchmark dataset used in a recent MICCAI segmentation challenge. In this context we show that MALP-EM is competitive for the segmentation of MR brain scans of healthy adults when compared to state-of-the-art automatic labelling techniques. To demonstrate the versatility of the proposed approach, we employed MALP-EM to segment 125 MR brain images into 134 regions from subjects who had sustained traumatic brain injury (TBI). We employ a protocol to assess segmentation quality if no manual reference labels are available. Based on this protocol, three independent, blinded raters confirmed on 13 MR brain scans with pathology that MALP-EM is superior to established label fusion techniques. We visually confirm the robustness of our segmentation approach on the full cohort and investigate the potential of derived symmetry-based imaging biomarkers that correlate with and predict clinically relevant variables in TBI such as the Marshall Classification (MC) or Glasgow Outcome Score (GOS). Specifically, we show that we are able to stratify TBI patients with favourable outcomes from non-favourable outcomes with 64.7% accuracy using acute-phase MR images and 66.8% accuracy using follow-up MR images. Furthermore, we are able to differentiate subjects with the presence of a mass lesion or midline shift from those with diffuse brain injury with 76.0% accuracy. The thalamus, putamen, pallidum and hippocampus are particularly affected. Their involvement predicts TBI disease progression.This work was partially funded under the 7th Framework Programme by the European Commission (http://cordis.europa.eu/ist/, TBIcare: http://www.tbicare.eu/, last accessed: 8 December 2014). The research was further supported by the National Institute for Health Research (NIHR) Biomedical Research Centre (BRC) based at Imperial College Healthcare NHS Trust and Imperial College London. AH is supported by the Department of Health via the NIHR comprehensive BRC award to Guy’s & St Thomas’ NHS Foundation Trust in partnership with King’s College London and Kings College Hospital NHS Foundation Trust. This work was further supported by a Medical Research Council (UK) Program Grant (Acute brain injury: heterogeneity of mechanisms, therapeutic targets and outcome effects [G9439390 ID 65883]), the UK National Institute of Health Research Biomedical Research Centre at Cambridge, the Technology Platform funding provided by the UK Department of Health and an EPSRC Pathways to Impact award. VFJN is supported by a Health Foundation/Academy of Medical Sciences Clinician Scientist Fellowship. DKM is supported by an NIHR Senior Investigator Award. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health. The funders had no role in study design, data collection and analyses, decision to publish, or preparation of the manuscript

    Theory of a cylindrical Langmuir probe parallel to the magnetic field and its calibration with interferometry

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    International audienceA theory for data interpretation is presented for a cylindrical Langmuir probe in plasma parallel to the magnetic field direction. The theory is tested in a linear low-temperature plasma device Aline, in a capacitive radio-frequency (RF) discharge. The probe is placed on a 3D manipulator and a position scan is performed. To exclude strong RF perturbations the probe is RF compensated. Using the theory electron densities are obtained from the current at the plasma potential, where no sheath is present. Results are calibrated by line-integrated density measurements of a 26.5 GHz microwave interferometer. Reasonable agreement is observed for probe and interferometer measurements. Furthermore, preceding, more general probe theory is compared to the one developed in the current work and the application limits are discussed

    Copy Number Variants in Patients with Severe Oligozoospermia and Sertoli-Cell-Only Syndrome

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    A genetic origin is estimated in 30% of infertile men with the common phenotypes of oligo- or azoospermia, but the pathogenesis of spermatogenic failure remains frequently obscure. To determine the involvement of Copy Number Variants (CNVs) in the origin of male infertility, patients with idiopathic severe oligozoospermia (N = 89), Sertoli-cell-only syndrome (SCOS, N = 37)) and controls with normozoospermia (N = 100) were analysed by array-CGH using the 244A/400K array sets (Agilent Technologies). The mean number of CNVs and the amount of DNA gain/loss were comparable between all groups. Ten recurring CNVs were only found in patients with severe oligozoospermia, three only in SCOS and one CNV in both groups with spermatogenic failure but not in normozoospermic men. Sex-chromosomal, mostly private CNVs were significantly overrepresented in patients with SCOS. CNVs found several times in all groups were analysed in a case-control design and four additional candidate genes and two regions without known genes were associated with SCOS (P<1×10−3). In conclusion, by applying array-CGH to study male infertility for the first time, we provide a number of candidate genes possibly causing or being risk factors for the men's spermatogenic failure. The recurring, patient-specific and private, sex-chromosomal CNVs as well as those associated with SCOS are candidates for further, larger case-control and re-sequencing studies
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