Nowadays, the demand for soft-biometric-based devices is increasing rapidly because of the huge use of electronics items such as mobiles, laptops and electronic gadgets in daily life. Recently, the healthcare department also emerged with soft-biometric technology, i.e., face biometrics, because the entire data, i.e., (gender, age, face expression and spoofing) of patients, doctors and other staff in hospitals is managed and forwarded through digital systems to reduce paperwork. This concept makes the relation friendlier between the patient and doctors and makes access to medical reports and treatments easier, anywhere and at any moment of life. In this paper, we proposed a new soft-biometric-based methodology for a secure biometric system because medical information plays an essential role in our life. In the proposed model, 5-layer U-Net-based architecture is used for face detection and Alex-Net-based architecture is used for classification of facial information i.e., age, gender, facial expression and face spoofing, etc. The proposed model outperforms the other state of art methodologies. The proposed methodology is evaluated and verified on six benchmark datasets i.e., NUAA Photograph Imposter Database, CASIA, Adience, The Images of Groups Dataset (IOG), The Extended Cohn-Kanade Dataset CK+ and The Japanese Female Facial Expression (JAFFE) Dataset. The proposed model achieved an accuracy of 94.17% for spoofing, 83.26% for age, 95.31% for gender and 96.9% for facial expression. Overall, the modification made in the proposed model has given better results and it will go a long way in the future to support soft-biometric based applications.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9317232 | PMC |
http://dx.doi.org/10.3390/s22145160 | DOI Listing |
Clin Genet
December 2024
Univ. Lille, CHU Lille, ULR7364 - RADEME - Maladies RAres du DEveloppement embryonnaire et du Métabolisme, CRMR Déficiences Intellectuelles de Causes Rares, Lille, France.
Intellectual Developmental Disorder with Dysmorphic Facies and Ptosis (IDDDFP) is a rare autosomal dominant syndrome caused by pathogenic variants in the BRPF1 gene, which is critical for chromatin regulation. This study expands the clinical and molecular spectrum of IDDDFP by analysing 29 new patients from 20 families with confirmed BRPF1 variants. Our cohort presented with a wide range of clinical features including developmental delay, intellectual disability (ID) and characteristic dysmorphic facial features such as ptosis, blepharophimosis and a broad nasal bridge.
View Article and Find Full Text PDFTissue Cell
December 2024
Department of Facial Features, 970 Hospital, Joint Service Support Force of the Chinese People's Liberation Army, Yantai, Shandong, China. Electronic address:
Allergic rhinitis (AR), common in children and adolescents, involves Lysophosphatidylcholine acyltransferase 1 (LPCAT1) catalyzing surfactant lipid biosynthesis and suppressing endoplasmic reticulum expression. However, the precise mechanism underlying the impact of LPCAT1 on epithelial cell damage in AR remains elusive. Hence, the present investigation elucidated the potential effect of LPCAT1 on epithelial cell damage in AR by inhibiting endoplasmic reticulum stress.
View Article and Find Full Text PDFEmotion
January 2025
Department of Psychology, University of New Hampshire.
We examined categorical processing biases in the perception and recognition of facial expressions of emotion across two studies. In both studies, participants first learned to discriminate between two ambiguous facial expressions of emotion selected from the middle of a continuous array of blended expressions (i.e.
View Article and Find Full Text PDFDev Biol
January 2025
The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, 3052, Australia; Department of Medical Biology, The University of Melbourne, Parkville, Victoria, 3052, Australia. Electronic address:
The MYST family histone acetyltransferase gene, KAT6B (MYST4, MORF, QKF) is mutated in two distinct human congenital disorders characterised by intellectual disability, facial dysmorphogenesis and skeletal abnormalities; Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome and Genitopatellar syndrome. Despite its requirement in normal skeletal development, the cellular and transcriptional effects of KAT6B in skeletogenesis have not been thoroughly studied. Here, we show that germline deletion of the Kat6b gene in mice causes premature ossification in vivo, resulting in shortened craniofacial elements and increased bone density, as well as shortened tibias with an expanded pre-hypertrophic layer, as compared to wild type controls.
View Article and Find Full Text PDFRev Neurosci
January 2025
557765 Network of Neurosurgery and Artificial Intelligence (NONAI), Universal Scientific Education and Research Network (USERN ), Tehran, Iran.
The recognition and classification of facial expressions using artificial intelligence (AI) presents a promising avenue for early detection and monitoring of neurodegenerative disorders. This narrative review critically examines the current state of AI-driven facial expression analysis in the context of neurodegenerative diseases, such as Alzheimer's and Parkinson's. We discuss the potential of AI techniques, including deep learning and computer vision, to accurately interpret and categorize subtle changes in facial expressions associated with these pathological conditions.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!