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NDRindex: a method for the quality assessment of single-cell RNA-Seq preprocessing data
BACKGROUND: Single-cell RNA sequencing can be used to fairly determine cell types, which is beneficial to the medical field, especially the many recent studies on COVID-19. Generally, single-cell RNA data analysis pipelines include data normalization, size reduction, and unsupervised clustering. How...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7738244/ https://www.ncbi.nlm.nih.gov/pubmed/33323107 http://dx.doi.org/10.1186/s12859-020-03883-x |
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author | Xiao, Ruiyu Lu, Guoshan Guo, Wanqian Jin, Shuilin |
author_facet | Xiao, Ruiyu Lu, Guoshan Guo, Wanqian Jin, Shuilin |
author_sort | Xiao, Ruiyu |
collection | PubMed |
description | BACKGROUND: Single-cell RNA sequencing can be used to fairly determine cell types, which is beneficial to the medical field, especially the many recent studies on COVID-19. Generally, single-cell RNA data analysis pipelines include data normalization, size reduction, and unsupervised clustering. However, different normalization and size reduction methods will significantly affect the results of clustering and cell type enrichment analysis. Choices of preprocessing paths is crucial in scRNA-Seq data mining, because a proper preprocessing path can extract more important information from complex raw data and lead to more accurate clustering results. RESULTS: We proposed a method called NDRindex (Normalization and Dimensionality Reduction index) to evaluate data quality of outcomes of normalization and dimensionality reduction methods. The method includes a function to calculate the degree of data aggregation, which is the key to measuring data quality before clustering. For the five single-cell RNA sequence datasets we tested, the results proved the efficacy and accuracy of our index. CONCLUSIONS: This method we introduce focuses on filling the blanks in the selection of preprocessing paths, and the result proves its effectiveness and accuracy. Our research provides useful indicators for the evaluation of RNA-Seq data. |
format | Online Article Text |
id | pubmed-7738244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77382442020-12-16 NDRindex: a method for the quality assessment of single-cell RNA-Seq preprocessing data Xiao, Ruiyu Lu, Guoshan Guo, Wanqian Jin, Shuilin BMC Bioinformatics Software BACKGROUND: Single-cell RNA sequencing can be used to fairly determine cell types, which is beneficial to the medical field, especially the many recent studies on COVID-19. Generally, single-cell RNA data analysis pipelines include data normalization, size reduction, and unsupervised clustering. However, different normalization and size reduction methods will significantly affect the results of clustering and cell type enrichment analysis. Choices of preprocessing paths is crucial in scRNA-Seq data mining, because a proper preprocessing path can extract more important information from complex raw data and lead to more accurate clustering results. RESULTS: We proposed a method called NDRindex (Normalization and Dimensionality Reduction index) to evaluate data quality of outcomes of normalization and dimensionality reduction methods. The method includes a function to calculate the degree of data aggregation, which is the key to measuring data quality before clustering. For the five single-cell RNA sequence datasets we tested, the results proved the efficacy and accuracy of our index. CONCLUSIONS: This method we introduce focuses on filling the blanks in the selection of preprocessing paths, and the result proves its effectiveness and accuracy. Our research provides useful indicators for the evaluation of RNA-Seq data. BioMed Central 2020-12-16 /pmc/articles/PMC7738244/ /pubmed/33323107 http://dx.doi.org/10.1186/s12859-020-03883-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Software Xiao, Ruiyu Lu, Guoshan Guo, Wanqian Jin, Shuilin NDRindex: a method for the quality assessment of single-cell RNA-Seq preprocessing data |
title | NDRindex: a method for the quality assessment of single-cell RNA-Seq preprocessing data |
title_full | NDRindex: a method for the quality assessment of single-cell RNA-Seq preprocessing data |
title_fullStr | NDRindex: a method for the quality assessment of single-cell RNA-Seq preprocessing data |
title_full_unstemmed | NDRindex: a method for the quality assessment of single-cell RNA-Seq preprocessing data |
title_short | NDRindex: a method for the quality assessment of single-cell RNA-Seq preprocessing data |
title_sort | ndrindex: a method for the quality assessment of single-cell rna-seq preprocessing data |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7738244/ https://www.ncbi.nlm.nih.gov/pubmed/33323107 http://dx.doi.org/10.1186/s12859-020-03883-x |
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