FIERCE: reconstructing dynamic trajectories from the differentiation potency of single cells.
basic_science · Level V
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- Record sourced from PubMed, PMID 42440340.
- Also identified by DOI 10.1093/bioinformatics/btag516.
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Abstract
Since the introduction of single-cell RNA sequencing (scRNA-seq), numerous computational approaches have been developed to reconstruct dynamic cellular processes from static transcriptional profiles. These methods order cells along continuous trajectories by assessing their similarity in the gene expression space. However, they rely on several assumptions, such as prior knowledge of the structure and directionality of the expected genealogy. These assumptions can limit their application to complex cellular systems with poorly understood developmental paths. To address this challenge, we introduce FIERCE (Framework for InfERence of veloCity of the Entropy), a novel computational pipeline designed to predict the changes in the differentiation potency of single cells during dynamic processes. Through a fully unsupervised approach, FIERCE enables the inference of cell lineages directly on the differentiation landscape of the biological system, thus eliminating the need for prior specification of developmental parameters. We demonstrate the efficacy of FIERCE by reconstructing three well-known mouse differentiation systems and by quantifying its accuracy on simulated data. FIERCE R package is available on GitHub at https://github.com/bicciatolab/FIERCE. Supplementary data are available at Bioinformatics online.