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Three-Dimensional Face Reconstruction from Uncalibrated Photographs: Application to Early Detection of Genetic Syndromes

机译:未校准照片的三维人脸重建:在遗传综合征的早期检测中的应用

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Facial analysis from photography supports the early identification of genetic syndromes, but clinically-acquired uncalibrated images suffer from image pose and illumination variability. Although 3D photography overcomes some of the challenges of 2D images, 3D scanners are not typically available. We present an optimization method for 3D face reconstruction from uncalibrated 2D photographs of the face using a novel statistical shape model of the infant face. First, our method creates an initial estimation of the camera pose for each 2D photograph using the average shape of the statistical model and a set of 2D facial landmarks. Second, it calculates the camera pose and the parameters of the statistical model by minimizing the distance between the projection of the estimated 3D face in the image plane of each camera and the observed 2D face geometry. Using the reconstructed 3D faces, we automatically extract a set of 3D geometric and appearance descriptors and we use them to train a classifier to identify facial dysmorphology associated with genetic syndromes. We evaluated our face reconstruction method on 3D photographs of 54 subjects (age range 0-3 years), and we obtained a point-to-surface error of 2.01 ± 0.54%, which was a significant improvement over 2.98 ± 0.64% using state-of-the-art methods (p < 0.001). Our classifier detected genetic syndromes from the reconstructed 3D faces from the 2D photographs with 100% sensitivity and 92.11% specificity.
机译:摄影的面部分析支持遗传综合征的早期识别,但是临床获得的未经校准的图像会遭受图像姿势和照明可变性的困扰。尽管3D摄影克服了2D图像的一些挑战,但通常不提供3D扫描仪。我们提出了一种使用婴儿脸部新型统计形状模型从未校准的2D照片中进行3D人脸重建的优化方法。首先,我们的方法使用统计模型的平均形状和一组2D面部地标为每张2D照片创建相机姿态的初始估计。其次,它通过最小化估计的3D人脸在每个相机的图像平面中的投影与观察到的2D人脸几何之间的距离,来计算相机的姿势和统计模型的参数。使用重建的3D人脸,我们会自动提取一组3D几何和外观描述符,并使用它们来训练分类器,以识别与遗传综合征相关的面部畸形。我们在54位受试者(年龄范围为0-3岁)的3D照片上评估了我们的脸部重构方法,得出的点对面误差为2.01±0.54%,与使用状态为2.98±0.64%相比,显着改善最先进的方法(p <0.001)。我们的分类器从2D照片的3D重构面孔中检测出遗传综合症,其敏感性为100%,特异性为92.11%。

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