Density-based detection of cell transition states to construct disparate and bifurcating trajectories.
- Publisher:
- OXFORD UNIV PRESS
- Publication Type:
- Journal Article
- Citation:
- Nucleic Acids Res, 2022, 50, (21), pp. e122
- Issue Date:
- 2022-11-28
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Lan, T | |
dc.contributor.author |
Hutvagner, G |
|
dc.contributor.author |
Zhang, X |
|
dc.contributor.author | Liu, T | |
dc.contributor.author | Wong, L | |
dc.contributor.author |
Li, J |
|
dc.date.accessioned | 2023-02-22T03:28:34Z | |
dc.date.available | 2022-09-01 | |
dc.date.available | 2023-02-22T03:28:34Z | |
dc.date.issued | 2022-11-28 | |
dc.identifier.citation | Nucleic Acids Res, 2022, 50, (21), pp. e122 | |
dc.identifier.issn | 0305-1048 | |
dc.identifier.issn | 1362-4962 | |
dc.identifier.uri | http://hdl.handle.net/10453/166307 | |
dc.description.abstract | Tree- and linear-shaped cell differentiation trajectories have been widely observed in developmental biologies and can be also inferred through computational methods from single-cell RNA-sequencing datasets. However, trajectories with complicated topologies such as loops, disparate lineages and bifurcating hierarchy remain difficult to infer accurately. Here, we introduce a density-based trajectory inference method capable of constructing diverse shapes of topological patterns including the most intriguing bifurcations. The novelty of our method is a step to exploit overlapping probability distributions to identify transition states of cells for determining connectability between cell clusters, and another step to infer a stable trajectory through a base-topology guided iterative fitting. Our method precisely re-constructed various benchmark reference trajectories. As a case study to demonstrate practical usefulness, our method was tested on single-cell RNA sequencing profiles of blood cells of SARS-CoV-2-infected patients. We not only re-discovered the linear trajectory bridging the transition from IgM plasmablast cells to developing neutrophils, and also found a previously-undiscovered lineage which can be rigorously supported by differentially expressed gene analysis. | |
dc.format | ||
dc.language | eng | |
dc.publisher | OXFORD UNIV PRESS | |
dc.relation | http://purl.org/au-research/grants/arc/DP180100120 | |
dc.relation.ispartof | Nucleic Acids Res | |
dc.relation.isbasedon | 10.1093/nar/gkac785 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 05 Environmental Sciences, 06 Biological Sciences, 08 Information and Computing Sciences | |
dc.subject.classification | Developmental Biology | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Single-Cell Analysis | |
dc.subject.mesh | SARS-CoV-2 | |
dc.subject.mesh | COVID-19 | |
dc.subject.mesh | Cell Differentiation | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Cell Differentiation | |
dc.subject.mesh | Single-Cell Analysis | |
dc.subject.mesh | COVID-19 | |
dc.subject.mesh | SARS-CoV-2 | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Single-Cell Analysis | |
dc.subject.mesh | SARS-CoV-2 | |
dc.subject.mesh | COVID-19 | |
dc.subject.mesh | Cell Differentiation | |
dc.title | Density-based detection of cell transition states to construct disparate and bifurcating trajectories. | |
dc.type | Journal Article | |
utslib.citation.volume | 50 | |
utslib.location.activity | England | |
utslib.for | 05 Environmental Sciences | |
utslib.for | 06 Biological Sciences | |
utslib.for | 08 Information and Computing Sciences | |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Engineering and Information Technology | |
pubs.organisational-group | /University of Technology Sydney/Strength - CHT - Health Technologies | |
pubs.organisational-group | /University of Technology Sydney/Strength - AAI - Advanced Analytics Institute Research Centre | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Engineering and Information Technology/School of Biomedical Engineering | |
pubs.organisational-group | /University of Technology Sydney/Centre for Health Technologies (CHT) | |
utslib.copyright.status | open_access | * |
dc.date.updated | 2023-02-22T03:27:11Z | |
pubs.issue | 21 | |
pubs.publication-status | Published | |
pubs.volume | 50 | |
utslib.citation.issue | 21 |
Abstract:
Tree- and linear-shaped cell differentiation trajectories have been widely observed in developmental biologies and can be also inferred through computational methods from single-cell RNA-sequencing datasets. However, trajectories with complicated topologies such as loops, disparate lineages and bifurcating hierarchy remain difficult to infer accurately. Here, we introduce a density-based trajectory inference method capable of constructing diverse shapes of topological patterns including the most intriguing bifurcations. The novelty of our method is a step to exploit overlapping probability distributions to identify transition states of cells for determining connectability between cell clusters, and another step to infer a stable trajectory through a base-topology guided iterative fitting. Our method precisely re-constructed various benchmark reference trajectories. As a case study to demonstrate practical usefulness, our method was tested on single-cell RNA sequencing profiles of blood cells of SARS-CoV-2-infected patients. We not only re-discovered the linear trajectory bridging the transition from IgM plasmablast cells to developing neutrophils, and also found a previously-undiscovered lineage which can be rigorously supported by differentially expressed gene analysis.
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