Biology subjects

Michiels, M.

Publications and source records attributed to Michiels, M..

3 recordsLinked to original sources

bioRxiv2020

Learning massive interpretable gene regulatory networks of the human brain by merging Bayesian Networks

We present the Fast Greedy Equivalence Search (FGES)-Merge, a new method for learning the structure of gene regulatory networks via merging locally learned Bayesian networks, based on the fast greedy equivalent search algorithm. The method is competitive with the state of the art in terms of the Matthews correlation coefficient, which takes into account both precision and recall, while also improving upon it in terms of speed, scaling up to tens of thousands of variables and being able to use empirical knowledge about the topological structure of gene regulatory networks. We apply this method to learning the gene regulatory network for the full human genome using data from samples of different brain structures (from the Allen Human Brain Atlas). Furthermore, this Bayesian network model should predict interactions between genes in a way that is clear to experts, following the current trends in explainable artificial intelligence. To achieve this, we also present a new open-access visualization tool that facilitates the exploration of massive networks and can aid in finding nodes of interest for experimental tests.

bioinformatics↗

bioRxiv2020

Electrophysiology prediction of single neurons based on their morphology

Electrophysiology data acquisition of single neurons represents a key factor for the understanding of neuronal dynamics. However, the traditional method to acquire this data is through patch-clamp technology, which presents serious scalability flaws due to its slowness and complexity to record at fine-grained spatial precision (dendrites and axon). In silico biophysical models are therefore created for simulating hundreds of experiments that would be impractical to recreate in vitro. The optimal way to create these models is based on the knowledge of the morphological and electrical features for each neuron. Since large-scale data acquisition is often unfeasible for electrical data, previous expert knowledge can be used but it must have an acceptable degree of similarity with the type of neurons that we are trying to model. Here, we present a data-driven machine learning approach to predict the electrophysiological features of single neurons in case of only having their morphology available. To solve this multi-output regression problem, we use an artificial neural network that has the particularity of providing a probability distribution for every output feature, to incorporate uncertainty. Input data to train the model is obtained from from the Allen Cell Types database. The electrical properties can depend on the morphology, whose acquisition technology is highly automated and scalable so there exist large data sets of them. We also provide integrations with the BluePyOpt library to create a biophysical model using the original morphology and the predicted electrical features. Finally, we connect the resulting biophysical model with the Geppetto UI software to run all the simulations in a sophisticated user interface.

neuroscience↗

bioRxiv2020

NeuroSuites-BNs: An open web framework for massive Bayesian networks focused on neuroscience

BayeSuites is the first web framework for learning, visualizing, and interpreting Bayesian networks (BNs) that can scale to tens of thousands of nodes while providing fast and friendly user experience. All the necessary features that enable this are reviewed in this paper; these features include scalability, extensibility, interoperability, ease of use, and interpretability. Scalability is the key factor in learning and processing massive networks within reasonable time; for a maintainable software open to new functionalities, extensibility and interoperability are necessary. Ease of use and interpretability are fundamental aspects of model interpretation, fairly similar to the case of the recent explainable artificial intelligence trend. We present the capabilities of our proposed framework by highlighting a real example of a BN learned from genomic data obtained from Allen Institute for Brain Science. The extensibility properties of the software are also demonstrated with the help of our BN-based probabilistic clustering implementation, together with another genomic-data example.

bioinformatics↗