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scGPS: Determining Cell States and Global Fate Potential of Subpopulations

Finding cell states and their transcriptional relatedness is a main outcome from analysing single-cell data. In developmental biology, determining whether cells are related in a differentiation lineage remains a major challenge. A seamless analysis pipeline from cell clustering to estimating the pro...

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Autores principales: Thompson, Michael, Matsumoto, Maika, Ma, Tianqi, Senabouth, Anne, Palpant, Nathan J., Powell, Joseph E., Nguyen, Quan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326972/
https://www.ncbi.nlm.nih.gov/pubmed/34349778
http://dx.doi.org/10.3389/fgene.2021.666771
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author Thompson, Michael
Matsumoto, Maika
Ma, Tianqi
Senabouth, Anne
Palpant, Nathan J.
Powell, Joseph E.
Nguyen, Quan
author_facet Thompson, Michael
Matsumoto, Maika
Ma, Tianqi
Senabouth, Anne
Palpant, Nathan J.
Powell, Joseph E.
Nguyen, Quan
author_sort Thompson, Michael
collection PubMed
description Finding cell states and their transcriptional relatedness is a main outcome from analysing single-cell data. In developmental biology, determining whether cells are related in a differentiation lineage remains a major challenge. A seamless analysis pipeline from cell clustering to estimating the probability of transitions between cell clusters is lacking. Here, we present Single Cell Global fate Potential of Subpopulations (scGPS) to characterise transcriptional relationship between cell states. scGPS decomposes mixed cell populations in one or more samples into clusters (SCORE algorithm) and estimates pairwise transitioning potential (scGPS algorithm) of any pair of clusters. SCORE allows for the assessment and selection of stable clustering results, a major challenge in clustering analysis. scGPS implements a novel approach, with machine learning classification, to flexibly construct trajectory connections between clusters. scGPS also has a feature selection functionality by network and modelling approaches to find biological processes and driver genes that connect cell populations. We applied scGPS in diverse developmental contexts and show superior results compared to a range of clustering and trajectory analysis methods. scGPS is able to identify the dynamics of cellular plasticity in a user-friendly workflow, that is fast and memory efficient. scGPS is implemented in R with optimised functions using C++ and is publicly available in Bioconductor.
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spelling pubmed-83269722021-08-03 scGPS: Determining Cell States and Global Fate Potential of Subpopulations Thompson, Michael Matsumoto, Maika Ma, Tianqi Senabouth, Anne Palpant, Nathan J. Powell, Joseph E. Nguyen, Quan Front Genet Genetics Finding cell states and their transcriptional relatedness is a main outcome from analysing single-cell data. In developmental biology, determining whether cells are related in a differentiation lineage remains a major challenge. A seamless analysis pipeline from cell clustering to estimating the probability of transitions between cell clusters is lacking. Here, we present Single Cell Global fate Potential of Subpopulations (scGPS) to characterise transcriptional relationship between cell states. scGPS decomposes mixed cell populations in one or more samples into clusters (SCORE algorithm) and estimates pairwise transitioning potential (scGPS algorithm) of any pair of clusters. SCORE allows for the assessment and selection of stable clustering results, a major challenge in clustering analysis. scGPS implements a novel approach, with machine learning classification, to flexibly construct trajectory connections between clusters. scGPS also has a feature selection functionality by network and modelling approaches to find biological processes and driver genes that connect cell populations. We applied scGPS in diverse developmental contexts and show superior results compared to a range of clustering and trajectory analysis methods. scGPS is able to identify the dynamics of cellular plasticity in a user-friendly workflow, that is fast and memory efficient. scGPS is implemented in R with optimised functions using C++ and is publicly available in Bioconductor. Frontiers Media S.A. 2021-07-19 /pmc/articles/PMC8326972/ /pubmed/34349778 http://dx.doi.org/10.3389/fgene.2021.666771 Text en Copyright © 2021 Thompson, Matsumoto, Ma, Senabouth, Palpant, Powell and Nguyen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Thompson, Michael
Matsumoto, Maika
Ma, Tianqi
Senabouth, Anne
Palpant, Nathan J.
Powell, Joseph E.
Nguyen, Quan
scGPS: Determining Cell States and Global Fate Potential of Subpopulations
title scGPS: Determining Cell States and Global Fate Potential of Subpopulations
title_full scGPS: Determining Cell States and Global Fate Potential of Subpopulations
title_fullStr scGPS: Determining Cell States and Global Fate Potential of Subpopulations
title_full_unstemmed scGPS: Determining Cell States and Global Fate Potential of Subpopulations
title_short scGPS: Determining Cell States and Global Fate Potential of Subpopulations
title_sort scgps: determining cell states and global fate potential of subpopulations
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326972/
https://www.ncbi.nlm.nih.gov/pubmed/34349778
http://dx.doi.org/10.3389/fgene.2021.666771
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