DNA methylation is a fundamental epigenetic modification involved in various biological processes and diseases. Analysis of DNA methylation data at a genome-wide and high-throughput level can provide insights into diseases influenced by epigenetics, such as cancer. Recent technological advances have led to the development of high-throughput approaches, such as genome-scale profiling, that allow for computational analysis of epigenetics. Deep learning (DL) methods are essential in facilitating computational studies in epigenetics for DNA methylation analysis. In this systematic review, we assessed the various applications of DL applied to DNA methylation data or multi-omics data to discover cancer biomarkers, perform classification, imputation and survival analysis. The review first introduces state-of-the-art DL architectures and highlights their usefulness in addressing challenges related to cancer epigenetics. Finally, the review discusses potential limitations and future research directions in this field.

Stochastic models can be difficult to test due to their complexity and randomness, yet their predictions are often used to make important decisions, so they need to be correct. We introduce a new search-based technique for testing implementations of stochastic models by maximising the differences between the implementation and a pseudo-oracle. Our technique reduces testing effort and enables discrepancies to be found that might otherwise be overlooked. We show the technique can identify differences challenging for humans to observe, and use it to help a new user understand implementation differences in a real model of a citrus disease (Huanglongbing) used to inform policy and research.