The practice of integrating images from two or more sensors collected from the same area or object is known as image fusion.The goal is to extract more spatial and spectral information from the resulting fused image t...The practice of integrating images from two or more sensors collected from the same area or object is known as image fusion.The goal is to extract more spatial and spectral information from the resulting fused image than from the component images.The images must be fused to improve the spatial and spectral quality of both panchromatic and multispectral images.This study provides a novel picture fusion technique that employs L0 smoothening Filter,Non-subsampled Contour let Transform(NSCT)and Sparse Representation(SR)followed by the Max absolute rule(MAR).The fusion approach is as follows:first,the multispectral and panchromatic images are divided into lower and higher frequency components using the L0 smoothing filter.Then comes the fusion process,which uses an approach that combines NSCT and SR to fuse low frequency components.Similarly,the Max-absolute fusion rule is used to merge high frequency components.Finally,the final image is obtained through the disintegration of fused low and high frequency data.In terms of correlation coefficient,Entropy,spatial frequency,and fusion mutual information,our method outperforms other methods in terms of image quality enhancement and visual evaluation.展开更多
Objectives To identify possible mutations in our previously cloned candidate gene for hereditary multiple exostoses type Ⅱ (EXT2) in affected members of EXT families so as to confirm that it is the disease causing ...Objectives To identify possible mutations in our previously cloned candidate gene for hereditary multiple exostoses type Ⅱ (EXT2) in affected members of EXT families so as to confirm that it is the disease causing gene. Methods The mutation was detected first by single strand conformational polymorphism(SSCP) of all coding exons of the candidate gene and then by sequencing analysis. Results After analyzing 37 patients from 20 Chinese EXT families by SSCP and DNA sequencing analysis, one 2 bp insertion mutation was identified in this candidate gene in affected members of an EXT family. This mutation resulted in the frameshift and generated a truncated gene product consisting of 105 amino acids. Conclusions The identification of the mutation in the candidate gene indicates that this novel gene is responsible for EXT2 (one of the disease causing gene of EXT).展开更多
文摘The practice of integrating images from two or more sensors collected from the same area or object is known as image fusion.The goal is to extract more spatial and spectral information from the resulting fused image than from the component images.The images must be fused to improve the spatial and spectral quality of both panchromatic and multispectral images.This study provides a novel picture fusion technique that employs L0 smoothening Filter,Non-subsampled Contour let Transform(NSCT)and Sparse Representation(SR)followed by the Max absolute rule(MAR).The fusion approach is as follows:first,the multispectral and panchromatic images are divided into lower and higher frequency components using the L0 smoothing filter.Then comes the fusion process,which uses an approach that combines NSCT and SR to fuse low frequency components.Similarly,the Max-absolute fusion rule is used to merge high frequency components.Finally,the final image is obtained through the disintegration of fused low and high frequency data.In terms of correlation coefficient,Entropy,spatial frequency,and fusion mutual information,our method outperforms other methods in terms of image quality enhancement and visual evaluation.
文摘Objectives To identify possible mutations in our previously cloned candidate gene for hereditary multiple exostoses type Ⅱ (EXT2) in affected members of EXT families so as to confirm that it is the disease causing gene. Methods The mutation was detected first by single strand conformational polymorphism(SSCP) of all coding exons of the candidate gene and then by sequencing analysis. Results After analyzing 37 patients from 20 Chinese EXT families by SSCP and DNA sequencing analysis, one 2 bp insertion mutation was identified in this candidate gene in affected members of an EXT family. This mutation resulted in the frameshift and generated a truncated gene product consisting of 105 amino acids. Conclusions The identification of the mutation in the candidate gene indicates that this novel gene is responsible for EXT2 (one of the disease causing gene of EXT).
