We present an efficient method for the fusion of medical captured images using different modalities that enhances the original images and combines the complementary information of the various modalities. The contourlet transform has mainly been employed as a fusion technique for images obtained from equal or different modalities. The limitation of directional information of dual-tree complex wavelet (DT-CWT) is rectified in dual-tree complex contourlet transform (DT-CCT) by incorporating directional filter banks (DFB) into the DT-CWT. The DT-CCT produces images with improved contours and textures, while the property of shift invariance is retained. To improve the fused image quality, we propose a new method for fusion rules based on principle component analysis (PCA) which depend on frequency component of DT-CCT coefficients (contourlet domain). For low frequency components, PCA method is adopted and for high frequency components, the salient features are picked up based on local energy. The final fusion image is obtained by directly applying inverse dual tree complex contourlet transform (IDT-CCT) to the fused low and high frequency components. The experimental results showed that the proposed method produces fixed image with extensive features on multimodality.
Chromosomal abnormalities are commonly associated with cancer, and their importance in the pathogenesis of the disease has been well recognized. Also recognized in recent years is the possibility that, together with chromosomal abnormalities, DNA ploidy of breast cancer aspirate cells, measured by image cytometric techniques, may correlate with prognosis of the disease. Here, we have examined the use of an artificial neural network to predict: 1) subclinical metastatic disease in the regional lymph nodes and 2) histological assessment, through the analysis of data obtained by image cytometric techniques of fine needle aspirates of breast tumors. The cellular features considered were: 1) DNA ploidy measured in terms of nuclear DNA content as well as by cell cycle distribution; 2) size of the S-phase fraction; and 3) nuclear pleomorphism. A further objective of the study was to analyze individual markers in terms of impact significance on predicting outcome in both cases. DNA ploidy, indicated by cell cycle distribution, was found markedly to influence the prediction of nodal spread of breast cancer, and nuclear pleomorphism to a lesser degree. Furthermore, a comparison between histological assessment and artificial neural network prediction shows a closer correlation between the neural approach and the development of further metastases as indicated in subsequent follow-up, than does histological assessment. These data demonstrate that artificial neural networks are capable of providing powerful and reliable indicators of possible lymph node metastasis, using measurements of cellular features alone.
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