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Duvina, M.

Publications and source records attributed to Duvina, M..

2 recordsLinked to original sources

SCITRAM: a Single-cell Integrated transcription regulation modeler for predicting master transcription factors

Single-cell omics technologies have provided unprecedented access to molecular cell heterogeneity, revolutionizing our understanding of complex living systems. Although generating such type of data has become a streamlined process, data processing still relies on command-line driven tools, or commercial solutions. Furthermore, single-cell transcriptomics analysis is usually reduced to stratifying cells on the grounds of gene expression signatures, while deconvolving gene regulatory programs (and their associated master transcription factors) responsible for cell heterogeneity are not classically addressed with the available tools, or performed under different data processing platforms. Herein, we present SCITRAM (Single-Cell Integrated TRAnscription regulation Modeler), a user-friendly stand-alone computational solution for predicting master transcription factors from single-cell transcriptomics data. SCITRAM first reconstructs a primary gene regulatory network and subsequently uses this network as template to model transcriptional cascades driven by the in-silico activation of transcription factors identified within the system. We validated SCITRAM performance across a variety of cell fate transition events including T cell exhaustion during solid tumor treatment, lineage stratification during pancreatic endocrinogenesis, as well as nervous tissue formation in cerebral organoid models. Overall, SCITRAM provides an accessible and integrated platform for processing (large amounts of) single-cell transcriptomics data, enabling the investigation of transcriptional regulatory programs and their master transcription factors without requiring a command-line driven environment.

bioinformatics↗

Enhancing spatial omics resolution by pseudo-interstitial pixels inference

MotivationSpatially resolved omics technologies are enhancing our understanding of tissues architecture. Despite major technological improvements, gaining in spatial resolution becomes experimentally expensive, while generating spatial landscapes at moderate resolution combined with computational methods for depixelating data represent a cost-effective strategy allowing to enlarge the number of experiments to be performed. ResultsWe have developed a computational strategy able to gain several-folds of resolution by inferring pseudo-interstitial pixels from their closest neighbors. This strategy has been validated in the context of public spatial transcriptomics data issued from melanoma, and human brain cortex tissue sections, by improving the identification of distinct tissue substructures. Furthermore, this methodology has been used for enhancing the resolution of consecutive sections collected from human brain organoids, as a way to demonstrate that a moderate resolution technology, combined with spatial depixelation processing allows to properly discern molecular tissue structures even in small tissues. Contactmmendoza@genoscope.cns.fr

bioinformatics↗