11 research outputs found
DeepASL: Enabling Ubiquitous and Non-Intrusive Word and Sentence-Level Sign Language Translation
There is an undeniable communication barrier between deaf people and people
with normal hearing ability. Although innovations in sign language translation
technology aim to tear down this communication barrier, the majority of
existing sign language translation systems are either intrusive or constrained
by resolution or ambient lighting conditions. Moreover, these existing systems
can only perform single-sign ASL translation rather than sentence-level
translation, making them much less useful in daily-life communication
scenarios. In this work, we fill this critical gap by presenting DeepASL, a
transformative deep learning-based sign language translation technology that
enables ubiquitous and non-intrusive American Sign Language (ASL) translation
at both word and sentence levels. DeepASL uses infrared light as its sensing
mechanism to non-intrusively capture the ASL signs. It incorporates a novel
hierarchical bidirectional deep recurrent neural network (HB-RNN) and a
probabilistic framework based on Connectionist Temporal Classification (CTC)
for word-level and sentence-level ASL translation respectively. To evaluate its
performance, we have collected 7,306 samples from 11 participants, covering 56
commonly used ASL words and 100 ASL sentences. DeepASL achieves an average
94.5% word-level translation accuracy and an average 8.2% word error rate on
translating unseen ASL sentences. Given its promising performance, we believe
DeepASL represents a significant step towards breaking the communication
barrier between deaf people and hearing majority, and thus has the significant
potential to fundamentally change deaf people's lives
Performance Evaluation of Deep Learning Algorithm Using High-End Media Processing Board in Real-Time Environment
Image processing-based artificial intelligence algorithm is a critical task, and the implementation requires a careful examination for the selection of the algorithm and the processing unit. With the advancement of technology, researchers have developed many algorithms to achieve high accuracy at minimum processing requirements. On the other hand, cost-effective high-end graphical processing units (GPUs) are now available to handle complex processing tasks. However, the optimum configurations of the various deep learning algorithms implemented on GPUs are yet to be investigated. In this proposed work, we have tested a Convolution Neural Network (CNN) based on You Only Look Once (YOLO) variants on NVIDIA Jetson Xavier to identify compatibility between the GPU and the YOLO models. Furthermore, the performance of the YOLOv3, YOLOv3-tiny, YOLOv4, and YOLOv5s models is evaluated during the training using our PowerEdge Dell R740 Server. We have successfully demonstrated that YOLOV5s is a good benchmark for object detection, classification, and traffic congestion using the Jetson Xavier GPU board. The YOLOv5s achieved an average precision of 95.9% among all YOLO variants and the highest success rate achieved is 98.89
Comparative Analysis of Photoplethysmography Signal Quality from Right and Left Index Fingers
Photoplethysmography (PPG) has emerged as an increasingly attractive signal for non-invasive physiological measurements, owing to its simplicity, cost-effectiveness, and broad applicability spanning cardiovascular to respiratory systems. The burgeoning interest in PPG signal processing has facilitated its extensive incorporation in wearable devices, thus stimulating active research in this field. The present study undertakes a comprehensive evaluation to discern the optimal index finger (right or left) for PPG data acquisition and subsequent filtration, appraised through the lens of the signal-to-noise ratio (SNR) of the filtered signal. An analysis conducted on signals contaminated with white Gaussian noise unveiled that the Savitzky-Golay filter (a polynomial filter) with a window size of three outperformed other window lengths, rendering the highest SNR. Among the Infinite Impulse Response (IIR) filters compared; the Chebyshev I filter emerged as superior. Interestingly, the right index finger consistently demonstrated a higher mean SNR across filters: 0.49% for the Savitzky-Golay filters, 4.32% for the Butterworth (order 6), 7.71% for the Chebyshev I (order 10), and 4.02% for the Chebyshev II (order 4), relative to the left index finger for PPG signals perturbed by white Gaussian noise. These findings provide an insightful perspective for future research and development in wearable devices, suggesting potential superiority of the right index finger for PPG signal acquisition and filtration
Molecular Diagnosis of Fragile X Syndrome in Subjects with Intellectual Disability of Unknown Origin: Implications of Its Prevalence in Regional Pakistan
<div><p>Fragile-X syndrome (FXS) is the most common form of inherited intellectual disability (ID) and affects 0.7–3.0% of intellectually compromised population of unknown etiology worldwide. It is mostly caused by repeat expansion mutations in the <i>FMR1</i> at chromosome Xq27.3. The present study aimed to develop molecular diagnostic tools for a better detection of FXS, to assess implementation of diagnostic protocols in a developing country and to estimate the prevalence of FXS in a cohort of intellectually disabled subjects from Pakistan. From a large pool of individuals with below normal IQ range, 395 subjects with intellectual disability of unknown etiology belonging to different regions of the country were recruited. Conventional-PCR, modified-PCR and Southern blot analysis methods were employed for the detection of CGG repeat polymorphisms in the <i>FMR1</i> gene. Initial screening with conventional-PCR identified 13 suspected patients. Subsequent investigations through modified PCR and Southern blot analyses confirmed the presence of the <i>FMR1</i> mutation, suggesting a prevalence of 3.5% and 2.8% (mean 3.3%) among the male and female ID patients, respectively. These diagnostic methods were further customized with the in-house conditions to offer robust screening of referral patients/families for diagnostics and genetic counseling. Prescreening and early diagnosis are crucial for designing a prudent strategy for the management of subjects with ID. Outcome of the study recommends health practitioners for implementation of molecular based FXS diagnosis in routine clinical practice to give a better care for patients similar to the ones included in the study.</p></div
A. Primer pair 1 PCR amplification products of FXS negative subjects (lanes 1–5).
<p>Agarose gel electrophoresis results of methylation specific PCR. <b>B.</b> Primer pair 3 gave amplification product of ~80bp of FXS positive subjects (lanes 2–4). <b>C.</b> Primer pair 4 did not give amplification of the FXS positive subjects (lanes 2&3) but yielded a product of ~300bp with FXS negative subjects (lane 4).</p
Clinical features of subjects with ID of unknown origin (n = 395, confirmed FXS = 13).
<p>* metacarpophalangeal.</p><p>Clinical features of subjects with ID of unknown origin (n = 395, confirmed FXS = 13).</p
Facial features of unrelated Fragile X patients.
<p>Facial features of unrelated Fragile X patients.</p
Southern blot analysis shows a normal female control (lane 2); premutation carrier females (lanes 3 and 7); methylation mosaic male (lane 4); full mutation female (lane 5); size mosaic males (lanes 6 and 8).
<p>1kb DNA size marker is shown in lane 1.</p
Selected pedigrees of FXS patients.
<p>Analyzed patients and carrier mothers are given identification numbers.</p