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Emile, J.-F.

Publications and source records attributed to Emile, J.-F..

2 recordsLinked to original sources

A deep learning-based multiscale integration of spatial omics with tumor morphology.

Spatial Transcriptomics (spTx) offers unprecedented insights into the spatial arrangement of the tumor microenvironment, tumor initiation/progression and identification of new therapeutic target candidates. However, spTx remains complex and unlikely to be routinely used in the near future. Hematoxylin and eosin (H&E) stained histological slides, on the other hand, are routinely generated for a large fraction of cancer patients. Here, we present a novel deep learning-based approach for multiscale integration of spTx with tumor morphology (MISO). We trained MISO to predict spTx from H&E on a new unpublished dataset of 72 10X Genomics Visium samples, and derived a novel estimate of the upper bound on the achievable performance. We demonstrate that MISO enables near single-cell-resolution, spatially-resolved gene expression prediction from H&E. In addition, MISO provides an effective patient representation framework that enables downstream predictive tasks such as molecular phenotyping or MSI prediction.

bioinformatics↗

PACpAInt: a deep learning approach to identify molecular subtypes of pancreatic adenocarcinoma on histology slides

Pancreatic ductal adenocarcinoma (PAC) is a highly heterogeneous and plastic tumor with different transcriptomic molecular subtypes that hold great prognostic and theranostic values. We developed PACpAInt, a multistep approach using deep learning models to determine tumor cell type and their molecular phenotype on routine histological preparation at a resolution enabling to decipher complete intratumor heterogeneity on a massive scale never achieved before. PACpAInt effectively identified molecular subtypes at the slide level in three validation cohorts and had an independent prognostic value. It identified an interslide heterogeneity within a case in 39% of tumors that impacted survival. Diving at the cell level, PACpAInt identified "pure" classical and basal-like main subtypes as well as an intermediary phenotype and hybrid tumors that co-carried both classical and basal-like phenotypes. These novel artificial intelligence-based subtypes, together with the proportion of basal-like cells within a tumor had a strong prognostic impact.

cancer biology↗