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- W2298083669 abstract "This work proposes a new DIC image fusion method that is well suited for merging angle information and extends the field of focus of DIC microscopic images. The proposed method only fuses information specifically linked to the epidermal cell layer of Arabidopsis leafs, thus avoiding clutter related to underlying cell layers. I. INTRODUCTION Differential interference contrast (DIC) microscopy is a type of optical microscopy that enhances the contrast in the image based on interferometry. This high contrast allows for the visualization of transparent cell walls, without requiring any staining. The major drawback of DIC microscopy is that it shows high contrast in one direction, the shear direction, but practically no contrast to the perpendicular direction [1]. While this is typically not an issue for a human operator, it seriously hampers the use of computer vision methods. Furthermore, in the leaf samples not all cells are located within the same focal plane. To overcome both the directional contrast and out-of-focus cells, we propose a novel fusion method that merges images with different shear directions and different focal depths." @default.
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- W2298083669 date "2014-01-01" @default.
- W2298083669 modified "2023-09-25" @default.
- W2298083669 title "Rotation and focal depth fusion of DIC microscopic images" @default.
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