Our research in computational biology and bioinformatics is mainly oriented towards the interpretation of large scale genomic and biological data in order to reveal the principles governing the molecular basis of life. Along these lines, we develop/utilize computational methods (empirical, statistical and machine/deep learning) that exploit any available type of biological information (e.g. macromolecular sequences and structures, gene expression data, biomedical literature) towards understanding biological systems, ranging from macromolecules and macromolecular complexes, to phenotypes.
In particular, we have a long-standing interest in the study of classes of non-globular proteins (e.g. transmembrane proteins, protein sequences with local compositional biases or repeats) and during the last decade we have focused our research on protein components of eukaryotic endomembrane systems, in particular nuclear pore complex subunits and components of the autophagy machinery. More specifically, we devise algorithms, methods/tools, databases and computer systems for: