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Sample area for surface roughness determination of skin surfaces

机译:用于确定皮肤表面粗糙度的样品区域

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A surface roughness algorithm has been developed and validated for determining roughness of psoriasis lesions. The algorithm extracts an estimated waviness surface from 3D rough surface of psoriasis lesion by applying high order polynomial surface fitting. Vertical deviations of the lesion are determined by subtracting its 3D surface from the estimated waviness surface. However, the performance of the algorithm is dependent on the area of skin surface. The objective of this paper is to determine the minimum area for optimal performance of the skin surface roughness algorithm. In the determined sample area, all significant roughness components must be covered for surface roughness determination. To find the minimum size of sampled area, skin surface roughness has been determined at several sampling area variations. Normal skin surfaces are used as input data in this evaluation. By referring to the plot of surface roughness dependency on sampled area variation, it can be shown that the threshold area is found to be 4.9×4.9 mm2 for skin surface roughness stability. Skin surface roughness variation is less for the sample areas larger than this threshold. However, there is a small surface roughness increment after the surface roughness stability. It is caused by fitting error at border regions of very large sample size.
机译:已经开发出一种表面粗糙度算法,并经过验证可以确定牛皮癣病变的粗糙度。该算法通过应用高阶多项式曲面拟合从牛皮癣病变的3D粗糙表面提取估计的波纹表面。病变的垂直偏差是通过从估计的波纹表面减去其3D表面来确定的。但是,算法的性能取决于皮肤表面的面积。本文的目的是确定皮肤表面粗糙度算法最佳性能的最小面积。在确定的样品区域中,必须覆盖所有重要的粗糙度成分才能确定表面粗糙度。为了找到最小的采样区域,已在多个采样区域变化下确定了皮肤表面粗糙度。在此评估中,正常皮肤表面用作输入数据。通过参考表面粗糙度对采样面积变化的依赖关系图,可以发现对于皮肤表面粗糙度稳定性,阈值面积被发现为4.9×4.9 mm 2 。对于大于此阈值的样本区域,皮肤表面粗糙度变化较小。但是,在表面粗糙度稳定之后,表面粗糙度增加很小。这是由于样本量很大的边界区域的拟合误差引起的。

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