Evidence map›Paper›PMID 30967106›Full record

ArticleBMC genomics2019

TSEE: an elastic embedding method to visualize the dynamic gene expression patterns of time series single-cell RNA sequencing data.

Shaokun An, Liang Ma, Lin Wan

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Article in BMC genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

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8citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Shaokun AnAcademy of Mathematics and Systems Science, Chinese Academy of Sciences, Beijing, 100190, China.
Liang MaBeijing Institute of Genomics, Chinese Academy of Sciences, Beijing, 100101, China. mal@big.ac.cn.
Lin WanAcademy of Mathematics and Systems Science, Chinese Academy of Sciences, Beijing, 100190, China. lwan@amss.ac.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTime series single-cell RNA sequencing (scRNA-seq) data are emerging. However, the analysis of time series scRNA-seq data could be compromised by 1) distortion created by assorted sources of data collection and generation across time samples and 2) inheritance of cell-to-cell variations by stochastic dynamic patterns of gene expression. This calls for the development of an algorithm able to visualize time series scRNA-seq data in order to reveal latent structures and uncover dynamic transition processes.

resultsIn this study, we propose an algorithm, termed time series elastic embedding (TSEE), by incorporating experimental temporal information into the elastic embedding (EE) method, in order to visualize time series scRNA-seq data. TSEE extends the EE algorithm by penalizing the proximal placement of latent points that correspond to data points otherwise separated by experimental time intervals. TSEE is herein used to visualize time series scRNA-seq datasets of embryonic developmental processed in human and zebrafish. We demonstrate that TSEE outperforms existing methods (e.g. PCA, tSNE and EE) in preserving local and global structures as well as enhancing the temporal resolution of samples. Meanwhile, TSEE reveals the dynamic oscillation patterns of gene expression waves during zebrafish embryogenesis.

conclusionsTSEE can efficiently visualize time series scRNA-seq data by diluting the distortions of assorted sources of data variation across time stages and achieve the temporal resolution enhancement by preserving temporal order and structure. TSEE uncovers the subtle dynamic structures of gene expression patterns, facilitating further downstream dynamic modeling and analysis of gene expression processes. The computational framework of TSEE is generalizable by allowing the incorporation of other sources of information.

Indexed as

AlgorithmsEmbryonic DevelopmentGene Expression Regulation, DevelopmentalAnimalsComputational BiologyGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansSequence Analysis, RNASingle-Cell AnalysisTime FactorsZebrafishCell fate decisionsElastic embeddingGene expression patternIn-group proportionNonlinear dimensionality reductionOscillationSingle-cell RNA sequencingTime seriesVisualization

Identifiers

PMID30967106
PMCPMC6456934

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.