Improving Deep Facial Phenotyping for Ultra-rare Disorder Verification Using Model Ensembles

被引:7
|
作者
Hustinx, Alexander [1 ]
Hellmann, Fabio [2 ]
Sumer, Omer [2 ]
Javanmardi, Behnam [1 ]
Andre, Elisabeth [2 ]
Krawitz, Peter [1 ]
Hsieh, Tzung-Chien [1 ]
机构
[1] Univ Bonn, Univ Hosp Bonn, Inst Genom Stat & Bioinformat, Bonn, Germany
[2] Univ Augsburg, Chair Human Ctr Artificial Intelligence, Augsburg, Germany
关键词
D O I
10.1109/WACV56688.2023.00499
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Rare genetic disorders affect more than 6% of the global population. Reaching a diagnosis is challenging because rare disorders are very diverse. Many disorders have recognizable facial features that are hints for clinicians to diagnose patients. Previous work, such as GestaltMatcher, utilized representation vectors produced by a DCNN similar to AlexNet to match patients in high-dimensional feature space to support "unseen" ultra-rare disorders. However, the architecture and dataset used for transfer learning in GestaltMatcher have become outdated. Moreover, a way to train the model for generating better representation vectors for unseen ultra-rare disorders has not yet been studied. Because of the overall scarcity of patients with ultra-rare disorders, it is infeasible to directly train a model on them. Therefore, we first analyzed the influence of replacing GestaltMatcher DCNN with a state-of-the-art face recognition approach, iResNet with ArcFace. Additionally, we experimented with different face recognition datasets for transfer learning. Furthermore, we proposed test-time augmentation, and model ensembles that mix general face verification models and models specific for verifying disorders to improve the disorder verification accuracy of unseen ultra-rare disorders. Our proposed ensemble model achieves state-of-the-art performance on both seen and unseen disorders. Code is available at github.com/igsb/GestaltMatcher-Arc.
引用
收藏
页码:5007 / 5017
页数:11
相关论文
共 50 条
  • [11] Hermansky-Pudlak Syndrome Type 2: A Case Report on an Ultra-Rare Disorder
    Alasmari, Badriah G.
    Wafa, Shady
    Tahir, Ali M.
    Aljubran, Abdullah
    Alfaifi, Adel
    Alsaab, Khulod
    Elzubair, Lina
    CUREUS JOURNAL OF MEDICAL SCIENCE, 2024, 16 (07)
  • [12] ASSESSMENT OF COST-EFFECTIVENESS RESULTS FROM ICER ULTRA-RARE DISORDER REVIEWS
    Arjunji, R.
    Venkitaramani, D.
    Wiesner, T.
    Maru, B.
    Dabbous, O.
    VALUE IN HEALTH, 2019, 22 : S338 - S338
  • [13] Studying ultra-rare variants in STX1A uncovers a novel neurodevelopmental disorder
    Esmeralda Villavicencio Gonzalez
    Ryan S. Dhindsa
    European Journal of Human Genetics, 2023, 31 : 973 - 974
  • [14] Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra-rare disease
    Adang, Laura A.
    Schlotawa, Lars
    Groeschel, Samuel
    Kehrer, Christiane
    Harzer, Klaus
    Staretz-Chacham, Orna
    Silva, Thiago Oliveira
    Schwartz, Ida Vanessa D.
    Gaertner, Jutta
    De Castro, Mauricio
    Costin, Carrie
    Montgomery, Esperanza Font
    Dierks, Thomas
    Radhakrishnan, Karthikeyan
    Ahrens-Nicklas, Rebecca C.
    JOURNAL OF INHERITED METABOLIC DISEASE, 2020, 43 (06) : 1298 - 1309
  • [15] Alström syndrome: an ultra-rare monogenic disorder as a model for insulin resistance, type 2 diabetes mellitus and obesity
    Francesca Dassie
    Francesca Favaretto
    Silvia Bettini
    Matteo Parolin
    Marina Valenti
    Felix Reschke
    Thomas Danne
    Roberto Vettor
    Gabriella Milan
    Pietro Maffei
    Endocrine, 2021, 71 : 618 - 625
  • [16] Parental perspectives of episodic irritability in an ultra-rare genetic disorder associated with NACC1
    Kelly Schoch
    Allyn McConkie-Rosell
    Nicole Walley
    Vikas Bhambhani
    Timothy Feyma
    Carolyn E. Pizoli
    Edward C. Smith
    Queenie K.-G. Tan
    Vandana Shashi
    Orphanet Journal of Rare Diseases, 18
  • [17] Parental perspectives of episodic irritability in an ultra-rare genetic disorder associated with NACC1
    Schoch, Kelly
    McConkie-Rosell, Allyn
    Walley, Nicole
    Bhambhani, Vikas
    Feyma, Timothy
    Pizoli, Carolyn E.
    Smith, Edward C.
    Tan, Queenie K. -G.
    Shashi, Vandana
    ORPHANET JOURNAL OF RARE DISEASES, 2023, 18 (01)
  • [18] Improving face verification using facial marks and deep CNN: IARPA Janus benchmark-A
    Riaz, Sidra
    Park, Unsang
    Natarajan, Prem
    IMAGE AND VISION COMPUTING, 2020, 104
  • [19] ECONOMIC MODEL FOR A GENE THERAPY IN AN ULTRA-RARE DISEASE: EXPERT VALIDATION OF APPROACH AND ASSUMPTIONS
    Sopena, L.
    Simons, C.
    Mumford, A.
    Bennison, C.
    Irvin, W.
    Paris, J. J.
    Buesch, K.
    VALUE IN HEALTH, 2022, 25 (01) : S79 - S79
  • [20] An Ultra-Rare Manifestation of an X-Linked Recessive Disorder: Duchenne Muscular Dystrophy in a Female Patient
    Szucs, Zsuzsanna
    Pinti, Eva
    Haltrich, Iren
    Szen, Orsolya Palne
    Nagy, Tibor
    Barta, Endre
    Mehes, Gabor
    Bidiga, Laszlo
    Torok, Olga
    Ujfalusi, Aniko
    Koczok, Katalin
    Balogh, Istvan
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (21)