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Visualizing scRNA-Seq Data at Population Scale with GloScope
Increasingly scRNA-Seq studies explore the heterogeneity of cell populations across different samples and its effect on an organism’s phenotype. However, relatively few bioinformatic methods have been developed which adequately address the variation between samples for such population-level analyses...
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/PMC10312527/ https://www.ncbi.nlm.nih.gov/pubmed/37398321 http://dx.doi.org/10.1101/2023.05.29.542786 |
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author | Wang, Hao Torous, William Gong, Boying Purdom, Elizabeth |
author_facet | Wang, Hao Torous, William Gong, Boying Purdom, Elizabeth |
author_sort | Wang, Hao |
collection | PubMed |
description | Increasingly scRNA-Seq studies explore the heterogeneity of cell populations across different samples and its effect on an organism’s phenotype. However, relatively few bioinformatic methods have been developed which adequately address the variation between samples for such population-level analyses. We propose a framework for representing the entire single-cell profile of a sample, which we call its GloScope representation. We implement GloScope on scRNA-Seq datasets from study designs ranging from 12 to over 300 samples. These examples demonstrate how GloScope allows researchers to perform essential bioinformatic tasks at the sample-level, in particular visualization and quality control assessment. |
format | Online Article Text |
id | pubmed-10312527 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-103125272023-07-01 Visualizing scRNA-Seq Data at Population Scale with GloScope Wang, Hao Torous, William Gong, Boying Purdom, Elizabeth bioRxiv Article Increasingly scRNA-Seq studies explore the heterogeneity of cell populations across different samples and its effect on an organism’s phenotype. However, relatively few bioinformatic methods have been developed which adequately address the variation between samples for such population-level analyses. We propose a framework for representing the entire single-cell profile of a sample, which we call its GloScope representation. We implement GloScope on scRNA-Seq datasets from study designs ranging from 12 to over 300 samples. These examples demonstrate how GloScope allows researchers to perform essential bioinformatic tasks at the sample-level, in particular visualization and quality control assessment. Cold Spring Harbor Laboratory 2023-06-01 /pmc/articles/PMC10312527/ /pubmed/37398321 http://dx.doi.org/10.1101/2023.05.29.542786 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use. |
spellingShingle | Article Wang, Hao Torous, William Gong, Boying Purdom, Elizabeth Visualizing scRNA-Seq Data at Population Scale with GloScope |
title | Visualizing scRNA-Seq Data at Population Scale with GloScope |
title_full | Visualizing scRNA-Seq Data at Population Scale with GloScope |
title_fullStr | Visualizing scRNA-Seq Data at Population Scale with GloScope |
title_full_unstemmed | Visualizing scRNA-Seq Data at Population Scale with GloScope |
title_short | Visualizing scRNA-Seq Data at Population Scale with GloScope |
title_sort | visualizing scrna-seq data at population scale with gloscope |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312527/ https://www.ncbi.nlm.nih.gov/pubmed/37398321 http://dx.doi.org/10.1101/2023.05.29.542786 |
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