Ada-VSR: Adaptive Video Super-Resolution with Meta-Learning

Most of the existing works in supervised spatio-temporal video super-resolution (STVSR) heavily rely on a large-scale external dataset consisting of paired low-resolution low-frame rate (LR-LFR)and high-resolution high-frame-rate (HR-HFR) videos. Despite their remarkable performance, these methods make a prior assumption that the low-resolution video is obtained by down-scaling the high-resolution video using a known degradation kernel, which does not hold in practical settings. Another problem with these methods is that they cannot exploit instance-specific internal information of video at testing time. Recently, deep internal learning approaches have gained attention due to their ability to utilize the instance-specific statistics of a video. However, these methods have a large inference time as they require thousands of gradient updates to learn the intrinsic structure of the data. In this work, we presentAdaptiveVideoSuper-Resolution (Ada-VSR) which leverages external, as well as internal, information through meta-transfer learning and internal learning, respectively. Specifically, meta-learning is employed to obtain adaptive parameters, using a large-scale external dataset, that can adapt quickly to the novel condition (degradation model) of the given test video during the internal learning task, thereby exploiting external and internal information of a video for super-resolution. The model trained using our approach can quickly adapt to a specific video condition with only a few gradient updates, which reduces the inference time significantly. Extensive experiments on standard datasets demonstrate that our method performs favorably against various state-of-the-art approaches.

SAGE: Sequential Attribute Generator for Analyzing Glioblastomas using Limited Dataset

While deep learning approaches have shown remarkable performance in many imaging tasks, most of these methods rely on availability of large quantities of data. Medical image data, however, is scarce and fragmented. Generative Adversarial Networks (GANs) have recently been very effective in handling such datasets by generating more data. If the datasets are very small, however, GANs cannot learn the data distribution properly, resulting in less diverse or low-quality results. One such limited dataset is that for the concurrent gain of 19 and 20 chromosomes (19/20 co-gain), a mutation with positive prognostic value in Glioblastomas (GBM). In this paper, we detect imaging biomarkers for the mutation to streamline the extensive and invasive prognosis pipeline. Since this mutation is relatively rare, i.e. small dataset, we propose a novel generative framework - the Sequential Attribute GEnerator (SAGE), that generates detailed tumor imaging features while learning from a limited dataset. Experiments show that not only does SAGE generate high quality tumors when compared to standard Deep Convolutional GAN (DC-GAN) and Wasserstein GAN with Gradient Penalty (WGAN-GP), it also captures the imaging biomarkers accurately.