Publications by authors named "Salome Carcy"

Article Synopsis
  • The "innate-like" T cell compartment, referred to as T, consists of diverse T cells that bridge innate and adaptive immunity and is analyzed using advanced techniques like single-cell RNA sequencing.
  • In human blood, most T cells exhibit an effector program driven by unique transcription factors, contrasting with conventional T cells, while varied developmental stages are observed in thymic T cells.
  • Unlike mice, human T cells do not form multiple effector subsets but show a mix of type 1 and type 17 effector potential, revealing key differences in immune regulation between species.
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The "innate-like" T cell compartment, known as T, represents a diverse group of T cells that straddle the boundary between innate and adaptive immunity, having the ability to mount rapid responses following activation. In mice, this ability is acquired during thymic development. We explored the transcriptional landscape of T compared to conventional T cells (T) in the human thymus and blood using single cell RNA sequencing and flow cytometry.

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Accurate generative statistical modeling of count data is of critical relevance for the analysis of biological datasets from high-throughput sequencing technologies. Important instances include the modeling of microbiome compositions from amplicon sequencing surveys and the analysis of cell type compositions derived from single-cell RNA sequencing. Microbial and cell type abundance data share remarkably similar statistical features, including their inherent compositionality and a natural hierarchical ordering of the individual components from taxonomic or cell lineage tree information, respectively.

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