As a high mortality disease, cancer seriously affects people's life and well-being. Reliance on pathologists to assess disease progression from pathological images is inaccurate and burdensome. Computer aided diagnosis (CAD) system can effectively assist diagnosis and make more credible decisions. However, a large number of labeled medical images that contribute to improve the accuracy of machine learning algorithm, especially for deep learning in CAD, are difficult to collect. Therefore, in this work, an improved few-shot learning method is proposed for medical image recognition. In addition, to make full use of the limited feature information in one or more samples, a feature fusion strategy is involved in our model. On the dataset of BreakHis and skin lesions, the experimental results show that our model achieved the classification accuracy of 91.22% and 71.20% respectively when only 10 labeled samples are given, which is superior to other state-of-the-art methods.

The computational methods of protein-protein interaction sites prediction can effectively avoid the shortcomings of high cost and time in traditional experimental approaches. However, the serious class imbalance between interface and non-interface residues on the protein sequences limits the prediction performance of these methods. This work therefore proposed a new strategy, NearMiss-based under-sampling for unbalancing datasets and Random Forest classification (NM-RF), to predict protein interaction sites. Herein, the residues on protein sequences were represented by the PSSM-derived features, hydropathy index (HI) and relative solvent accessibility (RSA). In order to resolve the class imbalance problem, an under-sampling method based on NearMiss algorithm is adopted to remove some non-interface residues, and then the random forest algorithm is used to perform binary classification on the balanced feature datasets. Experiments show that the accuracy of NM-RF model reaches 87.6% and 84.3% on Dtestset72 and PDBtestset164 respectively, which demonstrate the effectiveness of the proposed NM-RF method in differentiating the interface or non-interface residues.