42 research outputs found
A 3D Face Modelling Approach for Pose-Invariant Face Recognition in a Human-Robot Environment
Face analysis techniques have become a crucial component of human-machine
interaction in the fields of assistive and humanoid robotics. However, the
variations in head-pose that arise naturally in these environments are still a
great challenge. In this paper, we present a real-time capable 3D face
modelling framework for 2D in-the-wild images that is applicable for robotics.
The fitting of the 3D Morphable Model is based exclusively on automatically
detected landmarks. After fitting, the face can be corrected in pose and
transformed back to a frontal 2D representation that is more suitable for face
recognition. We conduct face recognition experiments with non-frontal images
from the MUCT database and uncontrolled, in the wild images from the PaSC
database, the most challenging face recognition database to date, showing an
improved performance. Finally, we present our SCITOS G5 robot system, which
incorporates our framework as a means of image pre-processing for face
analysis
Fitting a 3D Morphable Model to Edges: A Comparison Between Hard and Soft Correspondences
We propose a fully automatic method for fitting a 3D morphable model to
single face images in arbitrary pose and lighting. Our approach relies on
geometric features (edges and landmarks) and, inspired by the iterated closest
point algorithm, is based on computing hard correspondences between model
vertices and edge pixels. We demonstrate that this is superior to previous work
that uses soft correspondences to form an edge-derived cost surface that is
minimised by nonlinear optimisation.Comment: To appear in ACCV 2016 Workshop on Facial Informatic
3D Face Reconstruction from Light Field Images: A Model-free Approach
Reconstructing 3D facial geometry from a single RGB image has recently
instigated wide research interest. However, it is still an ill-posed problem
and most methods rely on prior models hence undermining the accuracy of the
recovered 3D faces. In this paper, we exploit the Epipolar Plane Images (EPI)
obtained from light field cameras and learn CNN models that recover horizontal
and vertical 3D facial curves from the respective horizontal and vertical EPIs.
Our 3D face reconstruction network (FaceLFnet) comprises a densely connected
architecture to learn accurate 3D facial curves from low resolution EPIs. To
train the proposed FaceLFnets from scratch, we synthesize photo-realistic light
field images from 3D facial scans. The curve by curve 3D face estimation
approach allows the networks to learn from only 14K images of 80 identities,
which still comprises over 11 Million EPIs/curves. The estimated facial curves
are merged into a single pointcloud to which a surface is fitted to get the
final 3D face. Our method is model-free, requires only a few training samples
to learn FaceLFnet and can reconstruct 3D faces with high accuracy from single
light field images under varying poses, expressions and lighting conditions.
Comparison on the BU-3DFE and BU-4DFE datasets show that our method reduces
reconstruction errors by over 20% compared to recent state of the art
Occlusion-aware 3D Morphable Models and an Illumination Prior for Face Image Analysis
Faces in natural images are often occluded by a variety of objects. We propose a fully automated, probabilistic and occlusion-aware 3D morphable face model adaptation framework following an analysis-by-synthesis setup. The key idea is to segment the image into regions explained by separate models. Our framework includes a 3D morphable face model, a prototype-based beard model and a simple model for occlusions and background regions. The segmentation and all the model parameters have to be inferred from the single target image. Face model adaptation and segmentation are solved jointly using an expectation-maximization-like procedure. During the E-step, we update the segmentation and in the M-step the face model parameters are updated. For face model adaptation we apply a stochastic sampling strategy based on the Metropolis-Hastings algorithm. For segmentation, we apply loopy belief propagation for inference in a Markov random field. Illumination estimation is critical for occlusion handling. Our combined segmentation and model adaptation needs a proper initialization of the illumination parameters. We propose a RANSAC-based robust illumination estimation technique. By applying this method to a large face image database we obtain a first empirical distribution of real-world illumination conditions. The obtained empirical distribution is made publicly available and can be used as prior in probabilistic frameworks, for regularization or to synthesize data for deep learning methods
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Sensitivity of simulated regional Arctic climate to the choice of coupled model domain
The climate over the Arctic has undergone changes in recent decades. In order to evaluate the coupled response of the Arctic system to external and internal forcing, our study focuses on the estimation of regional climate variability and its dependence on large-scale atmospheric and regional ocean circulations. A global ocean–sea ice model with regionally high horizontal resolution is coupled to an atmospheric regional model and global terrestrial hydrology model. This way of coupling divides the global ocean model setup into two different domains: one coupled, where the ocean and the atmosphere are interacting, and one uncoupled, where the ocean model is driven by prescribed atmospheric forcing and runs in a so-called stand-alone mode. Therefore, selecting a specific area for the regional atmosphere implies that the ocean–atmosphere system can develop ‘freely’ in that area, whereas for the rest of the global ocean, the circulation is driven by prescribed atmospheric forcing without any feedbacks. Five different coupled setups are chosen for ensemble simulations. The choice of the coupled domains was done to estimate the influences of the Subtropical Atlantic, Eurasian and North Pacific regions on northern North Atlantic and Arctic climate. Our simulations show that the regional coupled ocean–atmosphere model is sensitive to the choice of the modelled area. The different model configurations reproduce differently both the mean climate and its variability. Only two out of five model setups were able to reproduce the Arctic climate as observed under recent climate conditions (ERA-40 Reanalysis). Evidence is found that the main source of uncertainty for Arctic climate variability and its predictability is the North Pacific. The prescription of North Pacific conditions in the regional model leads to significant correlation with observations, even if the whole North Atlantic is within the coupled model domain. However, the inclusion of the North Pacific area into the coupled system drastically changes the Arctic climate variability to a point where the Arctic Oscillation becomes an ‘internal mode’ of variability and correlations of year-to-year variability with observational data vanish. In line with previous studies, our simulations provide evidence that Arctic sea ice export is mainly due to ‘internal variability’ within the Arctic region. We conclude that the choice of model domains should be based on physical knowledge of the atmospheric and oceanic processes and not on ‘geographic’ reasons. This is particularly the case for areas like the Arctic, which has very complex feedbacks between components of the regional climate system
Correction: Amitozyn Impairs Chromosome Segregation and Induces Apoptosis via Mitotic Checkpoint Activation
Correction: Amitozyn Impairs Chromosome Segregation and Induces Apoptosis via Mitotic Checkpoint Activation
General characterization of amitozyn effect on HeLa cells.
<p>(A) Cells were exposed to different concentrations of Am for 24 and 48 h and the percent of 2N and 4N cells in three independent experiments was estimated by FACScan and plotted in graph shown in the lower panel. ▪- percent of 2N cells after 24 h treatment; □ - percent of 4N cells after 24 h treatment; • - percent of 2N cells after 48 h treatment; - percent of 4N cells after 48 h treatment. (B) Kinetics of Am effect on HeLa cells. Cells were exposed to 125 µg/ml of Am for periods from 0 to 72 h and analyzed by FACScan. The percent of 2N and 4N cells from three independent experiments was plotted in graph shown at the bottom. ▴ - 2N cells in control; Δ- 4N cells in control; ♦ - 2N cells after treatment with Am; ◊ - 4N cells after treatment with Am. (C) FACScan analysis of mitotic cell ratio after Am treatment. The HeLa cells were exposed for 24 h to different Am concentrations, fixed with methanol, stained with PI and MPM2-FITC and analyzed by FACScan (upper panel). The average mitotic index of three independent experiments was plotted in the graph (lower panel). The Western blot inset shows the MPM2 level at indicated time points. (D) Reversibility of Am effect. The HeLa cells were synchronized in the G1/S phase by double thymidine block and released by medium addition (top row), exposed to Am (250 µg/ml) for 12 h with subsequent release in medium for 12 and 24 h (second row) or released in Am (250 µg/ml) during the entire experiment (last row). Cells were analyzed by FACScan as described in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0057461#s2" target="_blank">Materials and methods</a>.</p
Perturbation of cell signalling and mitotic checkpoint activation in HeLa cells upon Am treatment.
<p>HeLa cells were treated with 250 µg/ml Am for 12, 24 and 48 h. As a control (C) we used untreated cells grown for 48 h. Cell lysates were prepared as described in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0057461#s2" target="_blank">Materials and methods</a>, and the level of indicated proteins was analyzed by Western blot. Actin was used as loading control.</p
Anti-proliferative effect of amitozyn in different cell lines.
<p>Cells were treated with Am at indicated concentration for 72 h as described in Material and methods. Cells viability was determined by trypan blue exclusion.</p