论文标题
使用模型合奏改善对超稀有障碍验证的深层面部表型
Improving Deep Facial Phenotyping for Ultra-rare Disorder Verification Using Model Ensembles
论文作者
论文摘要
罕见的遗传疾病影响了超过6%的全球人口。达到诊断是具有挑战性的,因为罕见的疾病非常多样化。许多疾病具有可识别的面部特征,这是临床医生诊断患者的提示。先前的工作,例如Gestaltmatcher,使用了类似于Alexnet的DCNN生成的表示矢量,以匹配高维特征空间中的患者,以支持“看不见的”超稀有疾病。但是,用于传输GestaltMatcher中传输学习的架构和数据集已过时。此外,尚未研究一种训练模型以生成更好的表现向量的模型的方法。由于超稀有疾病的患者的总体稀缺性,直接训练模型就不可避免。因此,我们首先分析了用最先进的面部识别方法,带有Arcface的IRESNET代替Gestaltmatcher DCNN的影响。此外,我们还尝试了不同的面部识别数据集以进行转移学习。此外,我们提出了测试时间的增加,并模型组合将一般面部验证模型和特定于验证疾病的特定模型混合在一起,以提高看不见的超稀有疾病的疾病验证准确性。我们提出的合奏模型在可见和看不见的疾病上都取得了最先进的表现。
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 However, the architecture and dataset used for transfer learning in GestaltMatcher have become outdated.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.