A 3D Primary Vessel Reconstruction Framework with Serial Microscopy Images

被引:12
作者
Liang, Yanhui [1 ]
Wang, Fusheng [2 ]
Treanor, Darren [3 ]
Magee, Derek [4 ]
Teodoro, George [5 ]
Zhu, Yangyang [2 ]
Kong, Jun [1 ]
机构
[1] Emory Univ, Atlanta, GA 30322 USA
[2] SUNY Stony Brook, Stony Brook, NY 11794 USA
[3] Leeds Teaching Hosp NHS Trust, Leeds, W Yorkshire, England
[4] Univ Leeds, Leeds, W Yorkshire, England
[5] Univ Brasilia, Brasilia, DF, Brazil
来源
MEDICAL IMAGE COMPUTING AND COMPUTER-ASSISTED INTERVENTION, PT III | 2015年 / 9351卷
关键词
SEGMENTATION;
D O I
10.1007/978-3-319-24574-4_30
中图分类号
TP18 [人工智能理论];
学科分类号
081104 ; 0812 ; 0835 ; 1405 ;
摘要
Three dimensional microscopy images present significant potential to enhance biomedical studies. This paper presents an automated method for quantitative analysis of 3D primary vessel structures with histology whole slide images. With registered microscopy images of liver tissue, we identify primary vessels with an improved variational level set framework at each 2D slide. We propose a Vessel Directed Fitting Energy (VDFE) to provide prior information on vessel wall probability in an energy minimization paradigm. We find the optimal vessel cross-section associations along the image sequence with a two-stage procedure. Vessel mappings are first found between each pair of adjacent slides with a similarity function for four association cases. These bi-slide vessel components are further linked by Bayesian Maximum A Posteriori (MAP) estimation where the posterior probability is modeled as a Markov chain. The efficacy of the proposed method is demonstrated with 54 whole slide microscopy images of sequential sections from a human liver.
引用
收藏
页码:251 / 259
页数:9
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