redPATH: Reconstructing the Pseudo Development Time of Cell Lineages in Single-cell RNA-seq Data and Applications in Cancer

The recent advancement of single-cell RNA sequencing (scRNA-seq) technologies facilitates the study of cell lineages in developmental processes and cancer. In this study, we developed a computational method, called redPATH, to reconstruct the pseudo developmental time of cell lineages using a consen...

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Autores principales: Kaikun Xie, Zehua Liu, Ning Chen, Ting Chen
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Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/84f6976d27554d73bf95a2ea2bef2873
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spelling oai:doaj.org-article:84f6976d27554d73bf95a2ea2bef28732021-11-16T04:09:22ZredPATH: Reconstructing the Pseudo Development Time of Cell Lineages in Single-cell RNA-seq Data and Applications in Cancer1672-022910.1016/j.gpb.2020.06.014https://doaj.org/article/84f6976d27554d73bf95a2ea2bef28732021-04-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S167202292100019Xhttps://doaj.org/toc/1672-0229The recent advancement of single-cell RNA sequencing (scRNA-seq) technologies facilitates the study of cell lineages in developmental processes and cancer. In this study, we developed a computational method, called redPATH, to reconstruct the pseudo developmental time of cell lineages using a consensus asymmetric Hamiltonian path algorithm. Besides, we developed a novel approach to visualize the trajectory development and implemented visualization methods to provide biological insights. We validated the performance of redPATH by segmenting different stages of cell development on multiple neural stem cell and cancer datasets, as well as other single-cell transcriptome data. In particular, we identified a stem cell-like subpopulation in malignant glioma cells. These cells express known proliferative markers, such as GFAP, ATP1A2, IGFBPL1, and ALDOC, and remain silenced for quiescent markers such as ID3. Furthermore, we identified MCL1 as a significant gene that regulates cell apoptosis and CSF1R for reprogramming macrophages to control tumor growth. In conclusion, redPATH is a comprehensive tool for analyzing scRNA-seq datasets along the pseudo developmental time. redPATH is available at https://github.com/tinglabs/redPATH.Kaikun XieZehua LiuNing ChenTing ChenElsevierarticleSingle-cell pseudotime reconstructionConsensus Hamiltonian pathCell differentiationCell proliferationCell development and diseasesBiology (General)QH301-705.5ENGenomics, Proteomics & Bioinformatics, Vol 19, Iss 2, Pp 292-305 (2021)
institution DOAJ
collection DOAJ
language EN
topic Single-cell pseudotime reconstruction
Consensus Hamiltonian path
Cell differentiation
Cell proliferation
Cell development and diseases
Biology (General)
QH301-705.5
spellingShingle Single-cell pseudotime reconstruction
Consensus Hamiltonian path
Cell differentiation
Cell proliferation
Cell development and diseases
Biology (General)
QH301-705.5
Kaikun Xie
Zehua Liu
Ning Chen
Ting Chen
redPATH: Reconstructing the Pseudo Development Time of Cell Lineages in Single-cell RNA-seq Data and Applications in Cancer
description The recent advancement of single-cell RNA sequencing (scRNA-seq) technologies facilitates the study of cell lineages in developmental processes and cancer. In this study, we developed a computational method, called redPATH, to reconstruct the pseudo developmental time of cell lineages using a consensus asymmetric Hamiltonian path algorithm. Besides, we developed a novel approach to visualize the trajectory development and implemented visualization methods to provide biological insights. We validated the performance of redPATH by segmenting different stages of cell development on multiple neural stem cell and cancer datasets, as well as other single-cell transcriptome data. In particular, we identified a stem cell-like subpopulation in malignant glioma cells. These cells express known proliferative markers, such as GFAP, ATP1A2, IGFBPL1, and ALDOC, and remain silenced for quiescent markers such as ID3. Furthermore, we identified MCL1 as a significant gene that regulates cell apoptosis and CSF1R for reprogramming macrophages to control tumor growth. In conclusion, redPATH is a comprehensive tool for analyzing scRNA-seq datasets along the pseudo developmental time. redPATH is available at https://github.com/tinglabs/redPATH.
format article
author Kaikun Xie
Zehua Liu
Ning Chen
Ting Chen
author_facet Kaikun Xie
Zehua Liu
Ning Chen
Ting Chen
author_sort Kaikun Xie
title redPATH: Reconstructing the Pseudo Development Time of Cell Lineages in Single-cell RNA-seq Data and Applications in Cancer
title_short redPATH: Reconstructing the Pseudo Development Time of Cell Lineages in Single-cell RNA-seq Data and Applications in Cancer
title_full redPATH: Reconstructing the Pseudo Development Time of Cell Lineages in Single-cell RNA-seq Data and Applications in Cancer
title_fullStr redPATH: Reconstructing the Pseudo Development Time of Cell Lineages in Single-cell RNA-seq Data and Applications in Cancer
title_full_unstemmed redPATH: Reconstructing the Pseudo Development Time of Cell Lineages in Single-cell RNA-seq Data and Applications in Cancer
title_sort redpath: reconstructing the pseudo development time of cell lineages in single-cell rna-seq data and applications in cancer
publisher Elsevier
publishDate 2021
url https://doaj.org/article/84f6976d27554d73bf95a2ea2bef2873
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AT zehualiu redpathreconstructingthepseudodevelopmenttimeofcelllineagesinsinglecellrnaseqdataandapplicationsincancer
AT ningchen redpathreconstructingthepseudodevelopmenttimeofcelllineagesinsinglecellrnaseqdataandapplicationsincancer
AT tingchen redpathreconstructingthepseudodevelopmenttimeofcelllineagesinsinglecellrnaseqdataandapplicationsincancer
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