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Stephane Robin

Publications and source records attributed to Stephane Robin.

4 recordsLinked to original sources

AI Innovation and Firm Performance in the Medical Device Industry

Whether artificial intelligence pays off for the firms that build it into their products is hard to establish, because AI innovation is itself hard to observe. The medical technology sector is a rare exception: an AI-enabled device must obtain clearance from a national health authority before it can reach a patient, leaving a dated, firm-attributable record of AI innovation output that can be observed directly rather than proxied. We exploit this setting with a three-stage recursive model estimated on a novel firm-level dataset linking FDA premarket clearances, USPTO patents, Scopus publications, and Orbis financials, tracing the full innovation chain from external collaboration through AI device introduction to firm performance. We find that external AI research collaboration is a robust driver of AI device introduction across firm sizes and estimators, with a larger effect for small firms, consistent with external knowledge ties substituting for limited internal R&D capacity. Decomposing by partner type, the effect is largest for industry and clinical collaborations and smallest for academic ties, consistent with the former being closer to the regulatory and commercialisation process. Firms that bring AI devices to market display higher labour productivity, an effect robust for small firms and the full sample that holds under both sequential and joint maximum-likelihood estimation and accumulates across successive device introductions. Effects on profit margins are present but weaker and do not survive all specifications, a pattern consistent with competitive entry eroding pricing power as AI devices diffuse through the sector.

econ.GN

Inferring the presence and abundance of rare waterbirds species from scarce data

Abundance data are used in ecology for species monitoring and conservation. These count data often display several specific characteristics like numerous missing data, high variance, and a high proportion of zeros, particularly when monitoring rare species. We present a model that aims to impute missing data and estimate the effect of covariates on species presence and abundance. It is based on the log-normal Poisson model, which offers more flexibility in the variance of counts than a Poisson model. A latent variable is added for the overrepresentation of zeros in the data. The imputation of missing data is made possible by assuming that the latent variance matrix has low rank and the inclusion of covariates. \\ We demonstrate the identifiability in the presence of missing data. Since maximum likelihood inference is intractable, we use a variational expectation-maximization algorithm to infer the parameters. We provide an estimate of the asymptotic variance of the estimators and derive prediction intervals for the imputations, an estimate of the temporal trend, and a procedure for detecting a potential change in this trend. \\ We evaluate our imputations and associated prediction intervals using artificially degraded monitoring data set. We conclude with an illustration on a monitoring waterbirds data set.

stat.ME

Segmentor3IsBack: an R package for the fast and exact segmentation of Seq-data

Genome annotation is an important issue in biology which has long been addressed with gene prediction methods and manual experiments requiring biological expertise. The expanding Next Generation Sequencing technologies and their enhanced precision allow a new approach to the domain: the segmentation of RNA-Seq data to determine gene boundaries. Because of its almost linear complexity, we propose to use the Pruned Dynamic Programming Algorithm, which performances had been acknowledged for CGH arrays, for Seq-experiment outputs. This requires the adaptation of the algorithm to the negative binomial distribution with which we model the data. We show that if the dispersion in the signal is known, the PDP algorithm can be used and we provide an estimator for this dispersion. We then propose to estimate the number of segments, which can be associated to coding or non-coding regions of the genome, using an oracle penalty. We illustrate the results of our approach on a real data-set and show its good performance. Our algorithm is available as an R package on the CRAN repository.

stat.CO