TY - JOUR
T1 - AFLN-DGCL: Adaptive Feature Learning Network with Difficulty-Guided Curriculum Learning for skin lesion segmentation
AU - Tang, Peng
AU - Yan, Xintong
AU - Liang, Qiaokang
AU - Zhang, Dan
N1 - Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/10
Y1 - 2021/10
N2 - Background and problems: Automated skin lesion segmentation is a crucial step in the whole computer-aided (CAD) skin disease process. Recently, the fully convolutional network (FCN) has achieved outstanding performance on this task. However, it remains challenging because of three problems: (1) the difficult cases on dermoscopy images, including low contrast lesion, bubble and hair occlusion cases; (2) the overfitting problem of FCN-based methods that is caused by the imbalanced training of difficult samples and easy samples; (3) the over-segmentation problem of FCN-based methods. Method: This work proposes a new skin lesion segmentation framework. Specifically, feature representations from dermoscopy images are learned by the Adaptive Feature Learning Network (AFLN). An ensemble learning method is introduced to build a fusion model, enabling the AFLN model to capture the multi-scale information. We propose a Difficulty-Guided Curriculum Learning (DGCL) with step-wise training strategy to handle the overfitting problem caused by the imbalanced training. Finally, a Selecting-The-Biggest-Connected-Region (STBCR) is proposed to alleviate the over-segmentation problem of the fusion model. Experimental results: The method performance is compared using the same defined metrics (DICE, JAC, and ACC) with other state-of-the-art works on publicly available ISIC 2016, ISIC 2017, and ISIC 2018 databases, and results (0.931, 0.875, and 0.966), (0.881, 0.807, and 0.948), and (0.920, 0.856, and 0.966) illustrate its advantages. Conclusion: The excellent and robust performances on three public databases proved that our method has the potential to be applied to CAD skin diseases diagnosis.
AB - Background and problems: Automated skin lesion segmentation is a crucial step in the whole computer-aided (CAD) skin disease process. Recently, the fully convolutional network (FCN) has achieved outstanding performance on this task. However, it remains challenging because of three problems: (1) the difficult cases on dermoscopy images, including low contrast lesion, bubble and hair occlusion cases; (2) the overfitting problem of FCN-based methods that is caused by the imbalanced training of difficult samples and easy samples; (3) the over-segmentation problem of FCN-based methods. Method: This work proposes a new skin lesion segmentation framework. Specifically, feature representations from dermoscopy images are learned by the Adaptive Feature Learning Network (AFLN). An ensemble learning method is introduced to build a fusion model, enabling the AFLN model to capture the multi-scale information. We propose a Difficulty-Guided Curriculum Learning (DGCL) with step-wise training strategy to handle the overfitting problem caused by the imbalanced training. Finally, a Selecting-The-Biggest-Connected-Region (STBCR) is proposed to alleviate the over-segmentation problem of the fusion model. Experimental results: The method performance is compared using the same defined metrics (DICE, JAC, and ACC) with other state-of-the-art works on publicly available ISIC 2016, ISIC 2017, and ISIC 2018 databases, and results (0.931, 0.875, and 0.966), (0.881, 0.807, and 0.948), and (0.920, 0.856, and 0.966) illustrate its advantages. Conclusion: The excellent and robust performances on three public databases proved that our method has the potential to be applied to CAD skin diseases diagnosis.
KW - Adaptive feature learning network
KW - Dermoscopy images
KW - Difficulty-guided curriculum learning
KW - Skin lesion segmentation
UR - http://www.scopus.com/inward/record.url?scp=85109025257&partnerID=8YFLogxK
U2 - 10.1016/j.asoc.2021.107656
DO - 10.1016/j.asoc.2021.107656
M3 - Journal article
AN - SCOPUS:85109025257
SN - 1568-4946
VL - 110
JO - Applied Soft Computing
JF - Applied Soft Computing
M1 - 107656
ER -