The representational hierarchy in human and artificial visual systems in the presence of object-scene regularities.

Human vision is still largely unexplained. Computer vision made impressive progress on this front, but it is still unclear to which extent artificial neural networks approximate human object vision at the behavioral and neural levels. Here, we investigated whether machine object vision mimics the representational hierarchy of human object vision with an experimental design that allows testing within-domain representations for animals and scenes, as well as across-domain representations reflecting their real-world contextual regularities such as animal-scene pairs that often co-occur in the visual environment. We found that DCNNs trained in object recognition acquire representations, in their late processing stage, that closely capture human conceptual judgements about the co-occurrence of animals and their typical scenes. Likewise, the DCNNs representational hierarchy shows surprising similarities with the representational transformations emerging in domain-specific ventrotemporal areas up to domain-general frontoparietal areas. Despite these remarkable similarities, the underlying information processing differs. The ability of neural networks to learn a human-like high-level conceptual representation of object-scene co-occurrence depends upon the amount of object-scene co-occurrence present in the image set thus highlighting the fundamental role of training history. Further, although mid/high-level DCNN layers represent the category division for animals and scenes as observed in VTC, its information content shows reduced domain-specific representational richness. To conclude, by testing within- and between-domain selectivity while manipulating contextual regularities we reveal unknown similarities and differences in the information processing strategies employed by human and artificial visual systems.

Computational modelling of genome-scale metabolic networks and its application to CHO cell cultures.

Genome-scale metabolic models (GEMs) have become increasingly important in recent years. Currently, GEMs are the most accurate in silico representation of the genotype-phenotype link. They allow us to study complex networks from the systems perspective. Their application may drastically reduce the amount of experimental and clinical work, improve diagnostic tools and increase our understanding of complex biological phenomena. GEMs have also demonstrated high potential for the optimisation of bio-based production of recombinant proteins. Herein, we review the basic concepts, methods, resources and software tools used for the reconstruction and application of GEMs. We overview the evolution of the modelling efforts devoted to the metabolism of Chinese Hamster Ovary (CHO) cells. We present a case study on CHO cell metabolism under different amino acid depletions. This leads us to the identification of the most influential as well as essential amino acids in selected CHO cell lines.