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Journal article

A descriptive marker gene approach to single-cell pseudotime inference

Abstract:

Motivation

Pseudotime estimation from single-cell gene expression data allows the recovery of temporal information from otherwise static profiles of individual cells. Conventional pseudotime inference methods emphasize an unsupervised transcriptome-wide approach and use retrospective analysis to evaluate the behaviour of individual genes. However, the resulting trajectories can only be understood in terms of abstract geometric structures and not in terms of interpretable models of gene behaviour.

Results

Here we introduce an orthogonal Bayesian approach termed ‘Ouija’ that learns pseudotimes from a small set of marker genes that might ordinarily be used to retrospectively confirm the accuracy of unsupervised pseudotime algorithms. Crucially, we model these genes in terms of switch-like or transient behaviour along the trajectory, allowing us to understand why the pseudotimes have been inferred and learn informative parameters about the behaviour of each gene. Since each gene is associated with a switch or peak time the genes are effectively ordered along with the cells, allowing each part of the trajectory to be understood in terms of the behaviour of certain genes. We demonstrate that this small panel of marker genes can recover pseudotimes that are consistent with those obtained using the entire transcriptome. Furthermore, we show that our method can detect differences in the regulation timings between two genes and identify ‘metastable’ states—discrete cell types along the continuous trajectories—that recapitulate known cell types.

Availability and implementation

An open source implementation is available as an R package at http://www.github.com/kieranrcampbell/ouija and as a Python/TensorFlow package at http://www.github.com/kieranrcampbell/ouijaflow.

Supplementary information

Supplementary data are available at Bioinformatics online.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1093/bioinformatics/bty498

Authors


More by this author
Institution:
University of Oxford
Division:
Medical Sciences Division
Department:
Department of Physiology Anatomy and Genetics
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Human Genetics Wt Centre
Role:
Author
ORCID:
0000-0001-7615-8523


Publisher:
Oxford University Press
Journal:
Bioinformatics More from this journal
Volume:
35
Issue:
1
Pages:
28-35
Publication date:
2018-06-23
Acceptance date:
2018-06-20
DOI:
EISSN:
1460-2059
ISSN:
1367-4803
Pmid:
29939207


Language:
English
Pubs id:
pubs:859939
UUID:
uuid:59c899de-74f4-4af8-873f-50802edf22f0
Local pid:
pubs:859939
Source identifiers:
859939
Deposit date:
2019-01-30

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