Neural networks have complex structures, and thus it is hard to understand their inner workings and ensure correctness. To understand and debug convolutional neural networks (CNNs) we propose techniques for testing the channels of CNNs. We design FtGAN, an extension to GAN, that can generate test data with varying the intensity (i.e., sum of the neurons) of a channel of a target CNN. We also proposed a channel selection algorithm to find representative channels for testing. To efficiently inspect the target CNN’s inference computations, we define unexpectedness score, which estimates how similar the inference computation of the test data is to that of the training data. We evaluated FtGAN with five public datasets and showed that our techniques successfully identify defective channels in five different CNN models.

The accurate prediction of cancer drug sensitivity according to the multiomics profiles of individual patients is crucial for precision cancer medicine. However, the development of prediction models has been challenged by the complex crosstalk of input features and the resistance-dominant drug response information contained in public databases. In this study, we propose a novel multidrug response prediction framework, response-aware multitask prediction (RAMP), via a Bayesian neural network and restrict it by soft-supervised contrastive regularization. To utilize network embedding vectors as representation learning features for heterogeneous networks, we harness response-aware negative sampling, which applies cell line-drug response information to the training of network embeddings. RAMP overcomes the prediction accuracy limitation induced by the imbalance of trained response data based on the comprehensive selection and utilization of drug response features. When trained on the Genomics of Drug Sensitivity in Cancer dataset, RAMP achieved an area under the receiver operating characteristic curve > 89%, an area under the precision-recall curve > 59% and an $\textrm{F}_1$ score > 52% and outperformed previously developed methods on both balanced and imbalanced datasets. Furthermore, RAMP predicted many missing drug responses that were not included in the public databases. Our results showed that RAMP will be suitable for the high-throughput prediction of cancer drug sensitivity and will be useful for guiding cancer drug selection processes. The Python implementation for RAMP is available at https://github.com/hvcl/RAMP.

A handheld fluorometer for detecting blue/green fluorescence from small Stokes shift fluorophores is presented in this paper. Two novel techniques have been introduced to emulate far-field operation while operating in the near field. A sensitivity of 26 (seconds per decade of dilution) and a resolution of 0.01 (concentration units) was achieved for detection of Alexa Fluor 488.