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CellRank 2: unified fate mapping in multiview single-cell data

209
Citations
July 1, 2024
Published Date

Research Abstract & Technology Focus

Abstract
Single-cell RNA sequencing allows us to model cellular state dynamics and fate decisions using expression similarity or RNA velocity to reconstruct state-change trajectories; however, trajectory inference does not incorporate valuable time point information or utilize additional modalities, whereas methods that address these different data views cannot be combined or do not scale. Here we present CellRank 2, a versatile and scalable framework to study cellular fate using multiview single-cell data of up to millions of cells in a unified fashion. CellRank 2 consistently recovers terminal states and fate probabilities across data modalities in human hematopoiesis and endodermal development. Our framework also allows combining transitions within and across experimental time points, a feature we use to recover genes promoting medullary thymic epithelial cell formation during pharyngeal endoderm development. Moreover, we enable estimating cell-specific transcription and degradation rates from metabolic-labeling data, which we apply to an intestinal organoid system to delineate differentiation trajectories and pinpoint regulatory strategies.
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CellRank 2: unified fate mapping in multiview single-cell data

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What is the core focus of the research titled 'CellRank 2: unified fate mapping in multiview single-cell data'?

This literature focuses on: Abstract Single-cell RNA sequencing allows us to model cellular state dynamics and fate decisions using expression similarity or RNA velocity to reconstruct state-change trajectories; however, trajectory inference does not incorp...

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Yes, highly correlated activity was mapped. An entry titled 'CellRank 2: unified fate mapping in multiview single-cell data' discusses this: Abstract Single-cell RNA sequencing allows us to model cellular state dynamics and fate decisions using expression similarity or ...

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Yes, highly correlated activity was mapped. An entry titled 'Calculate multilple stats for two or more columns in R data.table' discusses this: An alternative where the function takes "all columns" (instead of individual columns). stats2 setNames(paste0(nm, c("_maximo", "_minimo"))) }, f...

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