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Obozinski, G.

Publications and source records attributed to Obozinski, G..

3 recordsLinked to original sources

Ensemble learning and ground-truth validation of synaptic connectivity inferred from spike trains

Probing the architecture of neuronal circuits and the principles that underlie their functional organization remains an important challenge of modern neurosciences. This holds true, in particular, for the inference of neuronal connectivity from large-scale extracellular recordings. Despite the popularity of this approach and a number of elaborate methods to reconstruct networks, the degree to which synaptic connections can be reconstructed from spike-train recordings alone remains controversial. Here, we provide a framework to probe and compare connectivity inference algorithms, using a combination of synthetic and empirical ground-truth data sets, obtained from simulations and parallel single-cell patch-clamp and high-density microelectrode array (HD-MEA) recordings in vitro. We find that reconstruction performance critically depends on the regularity of the recorded spontaneous activity, i.e., their dynamical regime, the type of connectivity, and the amount of available spike train data. We find gross differences between different algorithms, and many algorithms have difficulties in detecting inhibitory connections. We therefore introduce an ensemble artificial neural network (eANN) to improve connectivity inference. We train the eANN on the validated outputs of six established inference algorithms, and show how it improves network reconstruction accuracy and robustness. Overall, the eANN was robust across different dynamical regimes, with shorter recording time, and ameliorated the identification of synaptic connections, in particular inhibitory ones. Results indicated that the eANN also improved the topological characterization of neuronal networks. The presented methodology contributes to advancing the performance of inference algorithms and facilitates our understanding of how neuronal activity relates to synaptic connectivity. Author summaryThis study introduces an ensemble artificial neural network (eANN) to infer neuronal connectivity from multi-unit spike time recordings. We compare the eANN to previous algorithms and validate it using simulations and HD-MEA/patch-clamp datasets. The latter is obtained from three single-cell patch-clamp recordings and high-density microelectrode array (HD-MEA) measurements, in parallel. Our results demonstrate that the eANN outperforms all other algorithms across different dynamical regimes and provides a more accurate description of the underlying topological organization of the studied networks. We also provide a SHAP analysis of the trained eANN to understand which input features of the eANN contribute most to this superior performance. The eANN is a promising approach to improve connectivity inference from spike-train data.

neuroscience↗

A Graph Matching Approach to Tracking Neurons in Freely-Moving C. elegans

MotivationRecent advances in 3D microscopy allow for recording the neurons in freely-moving C. elegans at high frame rates. In order to read out calcium activity, it is necessary to track individual neurons from frame to frame. However, doing this by hand for tens of neurons in a single ten-minute recording requires more than a hundred hours. Moreover, most methods proposed in the literature for tracking neurons focus on immobilized or partially-immobilized worms and fail with freely-behaving worms. ResultsIn this paper we present an approach based on graph matching for tracking fluorescently-marked neurons in freely-moving C. elegans. Neurites (and sometimes neurons) can be oversegmented into pieces at the preprocessing phase; our algorithm allows several segments to match the same reference neuron or neurite. We demon-strate our method on three recordings. We find that with five labeled frames we can typically track the neurons and pieces of neurites with over 75% accuracy, with more reliable annotations for the most distinctive neurons. Availability and ImplementationThe code and preprocessed data will be made available upon publication. Contactcorinne.jones@epfl.ch

neuroscience↗

Deconvolution of ex-vivo drug screening data and bulk tissue expression predicts the abundance and viability of cancer cell subpopulations

Ex-vivo drug sensitivity screening allows the prediction of cancer treatment effectiveness in a personalized fashion. However, it only provides a readout on mixtures of cells, potentially occulting important information on clinically relevant cell subtypes. To address this shortcoming, we developed a machinelearning framework to decompose drug sensitivity recorded at the bulk level into cell subtype-specific drug sensitivity. We first determined that our method could decipher the cellular composition of bulk samples with top-ranking accuracy across five cancer types compared to state-of-the-art bulk deconvolution methods. We emphasize its effectiveness in the realm of Acute Myeloid Leukemia, where it appears to offer the most precise estimation of leukemic stem cell fractions across three test datasets and three patient cohorts. We then optimized an algorithm capable of estimating cell subtype- and single-cell-specific drug sensitivity, which we evaluated by performing in-vitro drug studies and in-depth simulations. We then applied our deconvolution strategy to the beatAML cohort dataset, currently the most extensive database of ex-vivo drug screening data. We developed a drug sensitivity profile tailored to specific cell subtypes, focusing on four therapeutic compounds predicted to target leukemic stem cells: the previously known midostaurin and A-674563, as well as SNS-032 and foretinib, which have not been previously linked to leukemic stem cells. Our work provides an attractive new computational tool for drug development and precision medicine.

bioinformatics↗