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LinRace: single cell lineage reconstruction using paired lineage barcode and gene expression data
Understanding how single cells divide and differentiate into different cell types in developed organs is one of the major tasks of developmental and stem cell biology. Recently, lineage tracing technology using CRISPR/Cas9 genome editing has enabled simultaneous readouts of gene expressions and line...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120693/ https://www.ncbi.nlm.nih.gov/pubmed/37090498 http://dx.doi.org/10.1101/2023.04.12.536601 |
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author | Pan, Xinhai Li, Hechen Putta, Pranav Zhang, Xiuwei |
author_facet | Pan, Xinhai Li, Hechen Putta, Pranav Zhang, Xiuwei |
author_sort | Pan, Xinhai |
collection | PubMed |
description | Understanding how single cells divide and differentiate into different cell types in developed organs is one of the major tasks of developmental and stem cell biology. Recently, lineage tracing technology using CRISPR/Cas9 genome editing has enabled simultaneous readouts of gene expressions and lineage barcodes in single cells, which allows for the reconstruction of the cell division tree, and even the detection of cell types and differentiation trajectories at the whole organism level. While most state-of-the-art methods for lineage reconstruction utilize only the lineage barcode data, methods that incorporate gene expression data are emerging, aiming to improve the accuracy of lineage reconstruction. However, effectively incorporating the gene expression data requires a reasonable model on how gene expression data changes along generations of divisions. Here, we present LinRace (Lineage Reconstruction with asymmetric cell division model), a method that integrates the lineage barcode and gene expression data using the asymmetric cell division model and infers cell lineage under a framework combining Neighbor Joining and maximum-likelihood heuristics. On both simulated and real data, LinRace outputs more accurate cell division trees than existing methods. Moreover, LinRace can output the cell states (cell types) of ancestral cells, which is rarely performed with existing lineage reconstruction methods. The information on ancestral cells can be used to analyze how a progenitor cell generates a large population of cells with various functionalities. LinRace is available at: https://github.com/ZhangLabGT/LinRace. |
format | Online Article Text |
id | pubmed-10120693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101206932023-04-22 LinRace: single cell lineage reconstruction using paired lineage barcode and gene expression data Pan, Xinhai Li, Hechen Putta, Pranav Zhang, Xiuwei bioRxiv Article Understanding how single cells divide and differentiate into different cell types in developed organs is one of the major tasks of developmental and stem cell biology. Recently, lineage tracing technology using CRISPR/Cas9 genome editing has enabled simultaneous readouts of gene expressions and lineage barcodes in single cells, which allows for the reconstruction of the cell division tree, and even the detection of cell types and differentiation trajectories at the whole organism level. While most state-of-the-art methods for lineage reconstruction utilize only the lineage barcode data, methods that incorporate gene expression data are emerging, aiming to improve the accuracy of lineage reconstruction. However, effectively incorporating the gene expression data requires a reasonable model on how gene expression data changes along generations of divisions. Here, we present LinRace (Lineage Reconstruction with asymmetric cell division model), a method that integrates the lineage barcode and gene expression data using the asymmetric cell division model and infers cell lineage under a framework combining Neighbor Joining and maximum-likelihood heuristics. On both simulated and real data, LinRace outputs more accurate cell division trees than existing methods. Moreover, LinRace can output the cell states (cell types) of ancestral cells, which is rarely performed with existing lineage reconstruction methods. The information on ancestral cells can be used to analyze how a progenitor cell generates a large population of cells with various functionalities. LinRace is available at: https://github.com/ZhangLabGT/LinRace. Cold Spring Harbor Laboratory 2023-05-14 /pmc/articles/PMC10120693/ /pubmed/37090498 http://dx.doi.org/10.1101/2023.04.12.536601 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Pan, Xinhai Li, Hechen Putta, Pranav Zhang, Xiuwei LinRace: single cell lineage reconstruction using paired lineage barcode and gene expression data |
title | LinRace: single cell lineage reconstruction using paired lineage barcode and gene expression data |
title_full | LinRace: single cell lineage reconstruction using paired lineage barcode and gene expression data |
title_fullStr | LinRace: single cell lineage reconstruction using paired lineage barcode and gene expression data |
title_full_unstemmed | LinRace: single cell lineage reconstruction using paired lineage barcode and gene expression data |
title_short | LinRace: single cell lineage reconstruction using paired lineage barcode and gene expression data |
title_sort | linrace: single cell lineage reconstruction using paired lineage barcode and gene expression data |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10120693/ https://www.ncbi.nlm.nih.gov/pubmed/37090498 http://dx.doi.org/10.1101/2023.04.12.536601 |
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