Neural activity sequences are ubiquitous in the brain and play pivotal roles in functions such as long-term memory formation and motor control. While conditions for storing and reactivating individual sequences have been thoroughly characterized, it remains unclear how multiple sequences may interact when activated simultaneously in recurrent neural networks. This question is especially relevant for weak sequences, comprised of fewer neurons, competing against strong sequences. Using a non-linear rate -based and a spiking model with discrete, pre-configured assemblies, we demonstrate that weak sequences can compensate for their competitive disadvantage either by increasing excitatory connections between subsequent assemblies or by cooperating with other co-active sequences. Further, our models suggest that such cooperation can negatively affect sequence speed unless subsequently active assemblies are paired. Our analysis characterizes the conditions for successful sequence progression in isolated, competing, and cooperating assembly sequences, and identifies the distinct contributions of recurrent and feed-forward projections. This proof-of-principle study shows how even disadvantaged sequences can be prioritized for reactivation, a process which has recently been implicated in hippocampal memory processing.

The plasticity of the conduction delay between neurons plays a fundamental role in learning temporal features that are essential for processing videos, speech, and many high-level functions. However, the exact underlying mechanisms in the brain for this modulation are still under investigation. Devising a rule for precisely adjusting the synaptic delays could eventually help in developing more efficient and powerful brain-inspired computational models. In this article, we propose an unsupervised bioplausible learning rule for adjusting the synaptic delays in spiking neural networks. We also provide the mathematical proofs to show the convergence of our rule in learning spatiotemporal patterns. Furthermore, to show the effectiveness of our learning rule, we conducted several experiments on random dot kinematogram and a subset of DVS128 Gesture data sets. The experimental results indicate the efficiency of applying our proposed delay learning rule in extracting spatiotemporal features in an STDP-based spiking neural network.

Reinforcement learning (RL) has recently regained popularity with major achievements such as beating the European game of Go champion. Here, for the first time, we show that RL can be used efficiently to train a spiking neural network (SNN) to perform object recognition in natural images without using an external classifier. We used a feedforward convolutional SNN and a temporal coding scheme where the most strongly activated neurons fire first, while less activated ones fire later, or not at all. In the highest layers, each neuron was assigned to an object category, and it was assumed that the stimulus category was the category of the first neuron to fire. If this assumption was correct, the neuron was rewarded, i.e., spike-timing-dependent plasticity (STDP) was applied, which reinforced the neuron's selectivity. Otherwise, anti-STDP was applied, which encouraged the neuron to learn something else. As demonstrated on various image data sets (Caltech, ETH-80, and NORB), this reward-modulated STDP (R-STDP) approach has extracted particularly discriminative visual features, whereas classic unsupervised STDP extracts any feature that consistently repeats. As a result, R-STDP has outperformed STDP on these data sets. Furthermore, R-STDP is suitable for online learning and can adapt to drastic changes such as label permutations. Finally, it is worth mentioning that both feature extraction and classification were done with spikes, using at most one spike per neuron. Thus, the network is hardware friendly and energy efficient.

BACKGROUND: Although different protein-protein physical interaction (PPI) datasets exist for Escherichia coli, no common methodology exists to integrate these datasets and extract reliable modules reflecting the existing biological process and protein complexes. Naïve Bayesian formula is the highly accepted method to integrate different PPI datasets into a single weighted PPI network, but detecting proper weights in such network is still a major problem. RESULTS: In this paper, we proposed a new methodology to integrate various physical PPI datasets into a single weighted PPI network in a way that the detected modules in PPI network exhibit the highest similarity to available functional modules. We used the co-expression modules as functional modules, and we shown that direct functional modules detected from Gene Ontology terms could be used as an alternative dataset. After running this integrating methodology over six different physical PPI datasets, orthologous high-confidence interactions from a related organism and two AP-MS PPI datasets gained high weights in the integrated networks, while the weights for one AP-MS PPI dataset and two other datasets derived from public databases have converged to zero. The majority of detected modules shaped around one or few hub protein(s). Still, a large number of highly interacting protein modules were detected which are functionally relevant and are likely to construct protein complexes. CONCLUSIONS: We provided a new high confidence protein complex prediction method supported by functional studies and literature mining.

BACKGROUND: The function of an RNA in cellular processes is directly related to its structure. The free energy of RNA structure in another important key to its function as only some structures with a specific level of free energy can take part in cellular reactions. Therefore, to perform a specific function, a particular RNA structure with specific level of free energy is required. For a given RNA structure, the goal of the RNA design problem is to design an RNA sequence that folds into the given structure. To mimic the biological features of RNA sequences and structures, some sequence and energy constraints should be considered in designing RNA. Although the level of free energy is important, it is not considered in the available approaches for RNA design problem. RESULTS: In this paper, we present a new version of our evolutionary algorithm for RNA design problem, entitled ERD, and extend it to handle some sequence and energy constraints. In the sequence constraints, one can restrict sequence positions to a fixed nucleotide or to a subset of nucleotides. As for the energy constraint, one can specify an interval for the free energy ranges of the designed sequences. We compare our algorithm with INFO-RNA, MODENA, NUPACK, and RNAiFold approaches for some artificial and natural RNA secondary structures and constraints. CONCLUSIONS: The results indicate that our algorithm outperforms the other mentioned approaches in terms of accuracy, speedup, divergency, nucleotides distribution, and similarity to the natural RNA sequences. Particularly, the designed RNA sequences in our method are much more reliable and similar to the natural counterparts. The generated sequences are more diverse and they have closer nucleotides distribution to the natural one. The ERD tool and web server are freely available at http://mostafa.ut.ac.ir/corna/erd-cons/ .

MOTIVATION: RNAs play fundamental roles in cellular processes. The function of an RNA is highly dependent on its 3D conformation, which is referred to as the RNA tertiary structure. Because the prediction or experimental determination of these structures is difficult, so many works focus on the problems associated with the RNA secondary structure. Here, we consider the RNA inverse folding problem, in which an RNA secondary structure is given as a target structure and the goal is to design an RNA sequence that folds into the target structure. In this article, we introduce a new evolutionary algorithm for the RNA inverse folding problem. Our algorithm, entitled Evolutionary RNA Design, generates a sequence whose minimum free energy structure is the same as the target structure. RESULTS: We compare our algorithm with INFO-RNA, MODENA, RNAiFold and NUPACK approaches for some biological test sets. The results presented in this article indicate that for longer structures, our algorithm performs better than the other mentioned algorithms in terms of the energy range, accuracy, speedup and nucleotide distribution. Particularly, the generated RNA sequences in our method are much more reliable and similar to the natural RNA sequences.