Biology subjects

Marin, J.-M.

Publications and source records attributed to Marin, J.-M..

5 recordsLinked to original sources

bioRxiv2024

Better confidence intervals in simulation-based inference

Simulation-based methods such as approximate Bayesian computation (ABC) are widely used to infer the evolutionary history of populations from molecular genetic data. We describe and evaluate a new iterative method of statistical inference about model parameters, which revisits the idea of inferring a likelihood surface using simulation when the likelihood function cannot be evaluated. It is based on combining the random forest machine learning method, and multivariate Gaussian mixture (MGM) models, in an effective inference workflow, here used to fit models with up to 15 variable parameters. In addition to the traditional assessment of precision in terms of bias and mean square error, we also evaluate the coverage of confidence intervals. The method is compared with approximate Bayesian computation using random forests (ABC-RF), a non-iterative method sharing some technical features with the proposed approach, across scenarios of historical demographic inference from population genetic data. It is also compared to another iterative method, sequential neural likelihood estimation (SNLE). These comparisons highlight the importance of an iterative workflow for exploring the parameter space efficiently. For equivalent simulation effort of the data-generating process, the new summary-likelihood method provides intervals whose coverage is better controlled than the marginal coverage of intervals provided by ABC with random forests, and than generally reported for ABC methods. The iterative workflow can also yield greater improvements in estimator precision when larger datasets are used.

bioinformatics↗

bioRxiv2022

Systematic analysis of the genomic features involved in the binding preferences of transcription factors

Transcription factors (TFs) orchestrate gene expression and are at the core of cell-specific phenotypes and functions. One given TF can therefore have different binding sites depending on cell type and conditions. However, the TF core motif, as represented by Position Weight Matrix for instance, are often, if not invariably, cell agnostic. Likewise, paralogous TFs recognize very similar motifs while binding different genomic regions. We propose a machine learning approach called TFscope aimed at identifying the DNA features explaining the binding differences observed between two ChIP-seq experiments targeting either the same TF in two cell types or treatments or two paralogous TFs. TFscope systematically investigates differences in i) core motif, ii) nucleotide environment around the binding site and iii) presence and location of co-factor motifs. It provides the main DNA features that have been detected, and the contribution of each of these features to explain the binding differences. TFscope has been applied to more than 350 pairs of ChIP-seq. Our experiments showed that the approach is accurate and that the genomic features distinguishing TF binding in two different settings vary according to the TFs considered and/or the conditions. Several samples are presented and discussed to illustrate these findings. For TFs in different cell types or with different treatments, co-factors and nucleotide environment often explain most of the binding-site differences, while for paralogous TFs, subtle differences in the core motif seem to be the main reason for the observed differences in our experiments. The source code (python), data and results of the experiments described in this article are available at https://gite.lirmm.fr/rromero/tfscope.

bioinformatics↗

bioRxiv2021

Joint inference of adaptive and demographic history from temporal population genomic data

Disentangling the effects of selection and drift is a long-standing problem in population genetics. Simulations show that pervasive selection may bias the inference of demography. Ideally, models for the inference of demography and selection should account for the interaction between these two forces. With simulation-based likelihood-free methods such as Approximate Bayesian Computation (ABC), demography and selection parameters can be jointly estimated. We propose to use the ABC-Random Forests framework to jointly infer demographic and selection parameters from temporal population genomic data (e.g. experimental evolution, monitored populations, ancient DNA). Our framework allowed the separation of demography (census size, N) from the genetic drift (effective population size, Ne) and the estimation of genome-wide parameters of selection. Selection parameters informed us about the adaptive potential of a population (the scaled mutation rate of beneficial mutations,{theta} b), the realized adaptation (the number of mutation under strong selection), and population fitness (genetic load). We applied this approach to a dataset of feral populations of honey bees (Apis mellifera) collected in California, and we estimated parameters consistent with the biology and the recent history of this species.

evolutionary biology↗

bioRxiv2019

A young age of subspecific divergence in the desert locust Schistocerca gregaria

AO_SCPLOWBSTRACTC_SCPLOWDating population divergence within species from molecular data and relating such dating to climatic and biogeographic changes is not trivial. Yet it can help formulating evolutionary hypotheses regarding local adaptation and future responses to changing environments. Key issues include statistical selection of a demographic and historical scenario among a set of possible scenarios, and estimation of the parameter(s) of interest under the chosen scenario. Such inferences greatly benefit from new statistical approaches including approximate Bayesian computation - Random Forest (ABC-RF), the latter providing reliable inference at a low computational cost, with the possibility to take into account prior knowledge on both biogeographical history and genetic markers. Here, we used ABC-RF, including independent information on evolutionary rate and pattern at microsatellite markers, to decipher the evolutionary history of the African arid-adapted pest locust, Schistocerca gregaria. We found that the evolutionary processes that have shaped the present geographical distribution of the species in two disjoint northern and southern regions of Africa were recent, dating back 2.6 Ky (90% CI: 0.9 - 6.6 Ky). ABC-RF inferences also supported a southern colonization of Africa from a low number of founders of northern origin. The inferred divergence history is better explained by the peculiar biology of S. gregaria, which involves a density-dependent swarming phase with some exceptional spectacular migrations, rather than a continuous colonization resulting from the continental expansion of open vegetation habitats during more ancient Quaternary glacial climatic episodes.

evolutionary biology↗

bioRxiv2017

Gene nucleotide composition accurately predicts expression and is linked to topological chromatin domains

Gene expression is orchestrated by distinct regulatory regions (e.g. promoters, enhancers, UTRs) to ensure a wide variety of cell types and functions. A challenge is to identify which regulatory regions are active, what are their associated features and how they work together in each cell type. Several approaches have tackled this problem by modeling gene expression based on epigenetic marks (e.g. ChIP-seq, methylation, DNase hypersensitivity), with the ultimate goal of identifying driving genomic regions and mutations that are clinically relevant in particular in precision medicine. However, these models rely on experimental data, which are limited to specific samples (even often to cell lines) and cannot be generated for all regulators and all patients. In addition, we show here that, although these approaches are accurate in predicting gene expression, their biological interpretation can be misleading. Finally these methods are not designed to capture potential regulation instructions present at the sequence level, before the binding of regulators or the opening of the chromatin. We develop here a method for predicting mRNA levels based solely on sequence features collected from distinct regulatory regions, which is as accurate as methods based on experimental data. Our approach confirms the importance of nucleotide composition in predicting gene expression and ranks regulatory regions according to their contribution. It also unveils strong influence of gene body sequence, in particular introns. We further provide evidence that the contribution of nucleotide content can be linked to co-regulations associated with genome 3D architecture and to associations of genes within topologically associated domains.

bioinformatics↗