TY - JOUR
T1 - Peripapillary atrophy detection by sparse biologically inspired feature manifold
AU - Cheng, Jun
AU - Tao, Dacheng
AU - Liu, Jiang
AU - Wong, Damon Wing Kee
AU - Tan, Ngan Meng
AU - Wong, Tien Yin
AU - Saw, Seang Mei
N1 - Funding Information:
Manuscript received July 31, 2012; accepted September 04, 2012. Date of publication September 10, 2012; date of current version November 27, 2012. This work was supported in part by the Agency for Science, Technology and Research, Singapore, under SERC grant 092-148-00731. Asterisk indicates corresponding author. *J. Cheng is with iMED Ocular Imaging Programme, Institute for Infocomm Research, Agency for Science, Technology and Research, Singapore (e-mail: jcheng@i2r.a-star.edu.sg).
PY - 2012
Y1 - 2012
N2 - Peripapillary atrophy (PPA) is an atrophy of pre-existing retina tissue. Because of its association with eye diseases such as myopia and glaucoma, PPA is an important indicator for diagnosis of these diseases. Experienced ophthalmologists are able to determine the presence of PPA using visual information from the retinal images. However, it is tedious, time consuming and subjective to examine all images especially in a screening program. This paper presents biologically inspired feature (BIF) for the automatic detection of PPA. BIF mimics the process of cortex for visual perception. In the proposed method, a focal region is segmented from the retinal image and the BIF is extracted. As BIF is an intrinsically low dimensional feature embedded in a high dimensional space, it is not suitable to measure the similarity between two BIFs directly based on the Euclidean distance. Therefore, it is necessary to obtain a suitable mapping to reduce the dimensionality. In this paper, we explore sparse transfer learning to transfer the label information from ophthalmologists to the sample distribution knowledge contained in all samples. Selective pair-wise discriminant analysis is used to define two strategies of sparse transfer learning: negative and positive sparse transfer learning. Experimental results show that negative sparse transfer learning is superior to the positive one for this task. The proposed BIF based approach achieves an accuracy of more than 90% in detecting PPA, much better than previous methods. It can be used to save the workload of ophthalmologists and thus reduce the diagnosis costs.
AB - Peripapillary atrophy (PPA) is an atrophy of pre-existing retina tissue. Because of its association with eye diseases such as myopia and glaucoma, PPA is an important indicator for diagnosis of these diseases. Experienced ophthalmologists are able to determine the presence of PPA using visual information from the retinal images. However, it is tedious, time consuming and subjective to examine all images especially in a screening program. This paper presents biologically inspired feature (BIF) for the automatic detection of PPA. BIF mimics the process of cortex for visual perception. In the proposed method, a focal region is segmented from the retinal image and the BIF is extracted. As BIF is an intrinsically low dimensional feature embedded in a high dimensional space, it is not suitable to measure the similarity between two BIFs directly based on the Euclidean distance. Therefore, it is necessary to obtain a suitable mapping to reduce the dimensionality. In this paper, we explore sparse transfer learning to transfer the label information from ophthalmologists to the sample distribution knowledge contained in all samples. Selective pair-wise discriminant analysis is used to define two strategies of sparse transfer learning: negative and positive sparse transfer learning. Experimental results show that negative sparse transfer learning is superior to the positive one for this task. The proposed BIF based approach achieves an accuracy of more than 90% in detecting PPA, much better than previous methods. It can be used to save the workload of ophthalmologists and thus reduce the diagnosis costs.
KW - Author
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UR - http://www.scopus.com/inward/record.url?scp=84870491726&partnerID=8YFLogxK
U2 - 10.1109/TMI.2012.2218118
DO - 10.1109/TMI.2012.2218118
M3 - Article
C2 - 22987511
AN - SCOPUS:84870491726
SN - 0278-0062
VL - 31
SP - 2355
EP - 2365
JO - IEEE Transactions on Medical Imaging
JF - IEEE Transactions on Medical Imaging
IS - 12
M1 - 6298012
ER -