This paper presents a method of computing a 2.1D sketch (i.e., layered image representation) from a single image with mixed Markov random field (MRF) under the Bayesian framework. Our model consists of three layers: t...This paper presents a method of computing a 2.1D sketch (i.e., layered image representation) from a single image with mixed Markov random field (MRF) under the Bayesian framework. Our model consists of three layers: the input image layer, the graphical representation layer of the computed 2D atomic regions and 3-degree junctions (such as T or arrow junctions), and the 2.1D sketch layer. There are two types of vertices in the graphical representation of the 2D entities: (i) regions, which act as the vertices found in traditional MRF, and (ii) address variables assigned to the terminators decomposed from the 3-degree junctions, which are a new type of vertices for the mixed MRF. We formulate the inference problem as computing the 2.1D sketch from the 2D graphical representation under the Bayesian framework, which consists of two components: (i) region layering/coloring based on the Swendsen-Wang cuts algorithm, which infers partial occluding order of regions, and (ii) address variable assignments based on Gibbs sampling, which completes the open bonds of the terminators of the 3-degree junctions. The proposed method is tested on the D-Order dataset, the Berkeley segmentation dataset and the Stanford 3D dataset. The experimental results show the efficiency and robustness of our approach. ? 2017 Beijing Institute of Aerospace Information.展开更多
Psoriasis is one of the most prevalent autoimmune skin diseases. However, its etiology and pathogencsis are still unclear. Over the last decade, omics-based technologies have been exten- sively utilized for biomarker ...Psoriasis is one of the most prevalent autoimmune skin diseases. However, its etiology and pathogencsis are still unclear. Over the last decade, omics-based technologies have been exten- sively utilized for biomarker discovery. As a result, some promising markers for psoriasis have been identified at the genome, transcriptome, proteome, and metabolome level. These discoveries have provided new insights into the underlying molecular mechanisms and signaling pathways in psoriasis pathogenesis. More importantly, some of these markers may prove useful in the diagnosis of psoriasis and in the prediction of disease progression once they have been validated. In this review, we summarize the most recent findings in psoriasis biomarker discovery. In addition, we will discuss several emerging technologies and their potential for novel blomarker discovery and diagnostics for psoriasis.展开更多
基金supported by the National Natural Science Foundation of China(61471343)the National Key Technology Research and Development Program of the Ministry of Science and Technology of China(2014BAK14B03)
文摘This paper presents a method of computing a 2.1D sketch (i.e., layered image representation) from a single image with mixed Markov random field (MRF) under the Bayesian framework. Our model consists of three layers: the input image layer, the graphical representation layer of the computed 2D atomic regions and 3-degree junctions (such as T or arrow junctions), and the 2.1D sketch layer. There are two types of vertices in the graphical representation of the 2D entities: (i) regions, which act as the vertices found in traditional MRF, and (ii) address variables assigned to the terminators decomposed from the 3-degree junctions, which are a new type of vertices for the mixed MRF. We formulate the inference problem as computing the 2.1D sketch from the 2D graphical representation under the Bayesian framework, which consists of two components: (i) region layering/coloring based on the Swendsen-Wang cuts algorithm, which infers partial occluding order of regions, and (ii) address variable assignments based on Gibbs sampling, which completes the open bonds of the terminators of the 3-degree junctions. The proposed method is tested on the D-Order dataset, the Berkeley segmentation dataset and the Stanford 3D dataset. The experimental results show the efficiency and robustness of our approach. ? 2017 Beijing Institute of Aerospace Information.
基金supported by the startup funds provided to TW by the University of Houston,USA
文摘Psoriasis is one of the most prevalent autoimmune skin diseases. However, its etiology and pathogencsis are still unclear. Over the last decade, omics-based technologies have been exten- sively utilized for biomarker discovery. As a result, some promising markers for psoriasis have been identified at the genome, transcriptome, proteome, and metabolome level. These discoveries have provided new insights into the underlying molecular mechanisms and signaling pathways in psoriasis pathogenesis. More importantly, some of these markers may prove useful in the diagnosis of psoriasis and in the prediction of disease progression once they have been validated. In this review, we summarize the most recent findings in psoriasis biomarker discovery. In addition, we will discuss several emerging technologies and their potential for novel blomarker discovery and diagnostics for psoriasis.
