2015
Authors
Gomes, AD; Ferreira, MFS; Moura, JP; Andre, RM; Silva, SO; Kobelke, J; Bierlich, J; Wondraczek, K; Schuster, K; Frazao, O;
Publication
24TH INTERNATIONAL CONFERENCE ON OPTICAL FIBRE SENSORS
Abstract
A new microstructured optical fiber is demonstrated to detect acetone evaporation by observing the time response of the reflected signal at 1550nm. The sensor consists on a caterpillar-like fiber, with a transversal microfluidic channel created with a Focused Ion Beam technique, spliced to a single-mode fiber. Different stages were visible between the dipping and the evaporation of acetone and of a mixture of water and acetone. It was also possible to detect the presence of water vapor.
2015
Authors
Ferreira, PM; Sequeira, AF; Rebelo, A;
Publication
PATTERN RECOGNITION AND IMAGE ANALYSIS (IBPRIA 2015)
Abstract
Fingerprint segmentation is a crucial step of an automatic fingerprint identification system, since an accurate segmentation promote both the elimination of spurious minutiae close to the foreground boundaries and the reduction of the computation time of the following steps. In this paper, a new, and more robust fingerprint segmentation algorithm is proposed. The main novelty is the introduction of a more robust binarization process in the framework, mainly based on the fuzzy C-means clustering algorithm. Experimental results demonstrate significant benchmark progress on three existing FVC datasets.
2015
Authors
Ferreira, C; Castro, P; Penas, S; Monteiro, A; Martins, L; Campilho, A; Azevedo, E; Polonia, J;
Publication
INTERNATIONAL JOURNAL OF STROKE
Abstract
2015
Authors
Sequeira, AF; Cardoso, JS;
Publication
SENSORS
Abstract
Fingerprint liveness detection methods have been developed as an attempt to overcome the vulnerability of fingerprint biometric systems to spoofing attacks. Traditional approaches have been quite optimistic about the behavior of the intruder assuming the use of a previously known material. This assumption has led to the use of supervised techniques to estimate the performance of the methods, using both live and spoof samples to train the predictive models and evaluate each type of fake samples individually. Additionally, the background was often included in the sample representation, completely distorting the decision process. Therefore, we propose that an automatic segmentation step should be performed to isolate the fingerprint from the background and truly decide on the liveness of the fingerprint and not on the characteristics of the background. Also, we argue that one cannot aim to model the fake samples completely since the material used by the intruder is unknown beforehand. We approach the design by modeling the distribution of the live samples and predicting as fake the samples very unlikely according to that model. Our experiments compare the performance of the supervised approaches with the semi-supervised ones that rely solely on the live samples. The results obtained differ from the ones obtained by the more standard approaches which reinforces our conviction that the results in the literature are misleadingly estimating the true vulnerability of the biometric system.
2015
Authors
Dashtbozorg, B; Mendonca, AM; Campilho, A;
Publication
COMPUTERS IN BIOLOGY AND MEDICINE
Abstract
Background: The optic disc (OD) centre and boundary are important landmarks in retinal images and are essential for automating the calculation of health biomarkers related with some prevalent systemic disorders, such as diabetes, hypertension, cerebrovascular and cardiovascular diseases. Methods: This paper presents an automatic approach for OD segmentation using a multiresolution sliding band filter (SBF). After the preprocessing phase, a low-resolution SBF is applied on a down-sampled retinal image and the locations of maximal filter response are used for focusing the analysis on a reduced region of interest (ROI). A high-resolution SBF is applied to obtain a set of pixels associated with the maximum response of the SBF, giving a coarse estimation of the OD boundary, which is regularized using a smoothing algorithm. Results: Our results are compared with manually extracted boundaries from public databases (ONHSD, MESSIDOR and INSPIRE-AVR datasets) outperforming recent approaches for OD segmentation. For the ONHSD, 44% of the results are classified as Excellent, while the remaining images are distributed between the Good (47%) and Fair (9%) categories. An average overlapping area of 83%, 89% and 85% is achieved for the images in ONHSD, MESSIDOR and INSPIR-AVR datasets, respectively, when comparing with the manually delineated OD regions. Discussion: The evaluation results on the images of three datasets demonstrate the better performance of the proposed method compared to recently published OD segmentation approaches and prove the independence of this method when from changes in image characteristics such as size, quality and camera field of view.
2015
Authors
Oliveira, LM; Carvalho, MI; Nogueira, EM; Tuchin, VV;
Publication
JOURNAL OF BIOMEDICAL OPTICS
Abstract
Part of the optical clearing study in biological tissues concerns the determination of the diffusion characteristics of water and optical clearing agents in the subject tissue. Such information is sufficient to characterize the time dependence of the optical clearing mechanisms-tissue dehydration and refractive index (RI) matching. We have used a simple method based on collimated optical transmittance measurements made from muscle samples under treatment with aqueous solutions containing different concentrations of ethylene glycol (EG), to determine the diffusion time values of water and EG in skeletal muscle. By representing the estimated mean diffusion time values from each treatment as a function of agent concentration in solution, we could identify the real diffusion times for water and agent. These values allowed for the calculation of the correspondent diffusion coefficients for those fluids. With these results, we have demonstrated that the dehydration mechanism is the one that dominates optical clearing in the first minute of treatment, while the RI matching takes over the optical clearing operations after that and remains for a longer time of treatment up to about 10 min, as we could see for EG and thin tissue samples of 0.5 mm. (C) 2015 Society of Photo-Optical Instrumentation Engineers (SPIE)
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