De novo prediction of RNA-protein interactions with graph neural networks.

RNA-binding proteins (RBPs) are key co- and post-transcriptional regulators of gene expression, playing a crucial role in many biological processes. Experimental methods like CLIP-seq have enabled the identification of transcriptome-wide RNA-protein interactions for select proteins; however, the time- and resource-intensive nature of these technologies call for the development of computational methods to complement their predictions. Here, we leverage recent, large-scale CLIP-seq experiments to construct a de novo predictor of RNA-protein interactions based on graph neural networks (GNN).

Challenges for machine learning in RNA-protein interaction prediction.

RNA-protein interactions have long being recognised as crucial regulators of gene expression. Recently, the development of scalable experimental techniques to measure these interactions has revolutionised the field, leading to the production of large-scale datasets which offer both opportunities and challenges for machine learning techniques. In this brief note, we will discuss some of the major stumbling blocks towards the use of machine learning in computational RNA biology, focusing specifically on the problem of predicting RNA-protein interactions from next-generation sequencing data.

Action-based Modeling of Complex Networks.

Complex networks can model a wide range of complex systems in nature and society, and many algorithms (network generators) capable of synthesizing networks with few and very specific structural characteristics (degree distribution, average path length, etc.) have been developed. However, there remains a significant lack of generators capable of synthesizing networks with strong resemblance to those observed in the real-world, which can subsequently be used as a null model, or to perform tasks such as extrapolation, compression and control.