20 research outputs found
A multi-biometric iris recognition system based on a deep learning approach
YesMultimodal biometric systems have been widely
applied in many real-world applications due to its ability to
deal with a number of significant limitations of unimodal
biometric systems, including sensitivity to noise, population
coverage, intra-class variability, non-universality, and
vulnerability to spoofing. In this paper, an efficient and
real-time multimodal biometric system is proposed based
on building deep learning representations for images of
both the right and left irises of a person, and fusing the
results obtained using a ranking-level fusion method. The
trained deep learning system proposed is called IrisConvNet
whose architecture is based on a combination of Convolutional
Neural Network (CNN) and Softmax classifier to
extract discriminative features from the input image without
any domain knowledge where the input image represents
the localized iris region and then classify it into one of N
classes. In this work, a discriminative CNN training scheme
based on a combination of back-propagation algorithm and
mini-batch AdaGrad optimization method is proposed for
weights updating and learning rate adaptation, respectively.
In addition, other training strategies (e.g., dropout method,
data augmentation) are also proposed in order to evaluate
different CNN architectures. The performance of the proposed
system is tested on three public datasets collected
under different conditions: SDUMLA-HMT, CASIA-Iris-
V3 Interval and IITD iris databases. The results obtained
from the proposed system outperform other state-of-the-art
of approaches (e.g., Wavelet transform, Scattering transform,
Local Binary Pattern and PCA) by achieving a Rank-1 identification rate of 100% on all the employed databases
and a recognition time less than one second per person
Deep Eyedentification: Biometric Identification using Micro-Movements of the Eye
We study involuntary micro-movements of the eye for biometric identification.
While prior studies extract lower-frequency macro-movements from the output of
video-based eye-tracking systems and engineer explicit features of these
macro-movements, we develop a deep convolutional architecture that processes
the raw eye-tracking signal. Compared to prior work, the network attains a
lower error rate by one order of magnitude and is faster by two orders of
magnitude: it identifies users accurately within seconds
Experimental and numerical studies on the effect of deep rolling on bending fretting fatigue resistance of Al7075
In Situ Laboratory-Based Transmission X-Ray Microscopy and Tomography of Material Deformation at the Nanoscale
Features Subset Selection using Improved Teaching Learning based Optimisation (ITLBO) Algorithms for Iris Recognition
Potential Role of Perilacunar Remodeling in the Progression of Osteoporosis and Implications on Age-Related Decline in Fracture Resistance of Bone
Impact of BRCA1 and BRCA2 variants on splicing: clues from an allelic imbalance study
Nearly one-half of BRCA1 and BRCA2 sequence variations are variants of uncertain significance (VUSs) and are candidates for splice alterations for example, by disrupting/creating splice sites. As out-of-frame splicing defects lead to a marked reduction of the level of the mutant mRNA cleared through nonsense-mediated mRNA decay, a cDNA-based test was developed to show the resulting allelic imbalance (AI). Fifty-four VUSs identified in 53 hereditary breast/ovarian cancer (HBOC) patients without BRCA1/2 mutation were included in the study. Two frequent exonic single-nucleotide polymorphisms on both BRCA1 and BRCA2 were investigated by using a semiquantitative single-nucleotide primer extension approach and the cDNA allelic ratios obtained were corrected using genomic DNA ratios from the same sample. A total of five samples showed AI. Subsequent transcript analyses ruled out the implication of VUS on AI and identified a deletion encompassing BRCA2 exons 12 and 13 in one sample. No sequence abnormality was found in the remaining four samples, suggesting implication of cis- or trans-acting factors in allelic expression regulation that might be disease causative in these HBOC patients. Overall, this study showed that AI screening is a simple way to detect deleterious splicing defects and that a major role for VUSs and deep intronic mutations in splicing anomalies is unlikely in BRCA1/2 genes. Methods to analyze gene expression and identify regulatory elements in BRCA1/2 are now needed to complement standard approaches to mutational analysis
