Evidence map›Paper›PMID 33323107›Full record

ArticleBMC bioinformatics2020

NDRindex: a method for the quality assessment of single-cell RNA-Seq preprocessing data.

Ruiyu Xiao, Guoshan Lu, Wanqian Guo, Shuilin Jin

Abstract read
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ruiyu XiaoSchool of Computer Science and Technology, Harbin Institute of Technology, Zhejiang, China.
Guoshan LuSchool of Computer Science and Technology, Harbin Institute of Technology, Zhejiang, China.
Wanqian GuoState Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin, China.
Shuilin JinState Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin, China. jinsl@hit.edu.cn.ORCID http://orcid.org/0000-0002-2318-432X

Funding

National Natural Science Foundation of China 11971130Open Project of State Key Laboratory of Urban Water Resource and Environment of Harbin Institute of Technology ES201602
6 · The paper itself

Abstract

backgroundSingle-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.

resultsWe 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.

conclusionsThis 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.

Indexed as

Cluster AnalysisComputational BiologyCOVID-19Databases, Nucleic AcidHumansRNA-SeqSARS-CoV-2Dimension reductionNormalizationPreprocess pathRNA-seqSingle-cell

Identifiers

PMID33323107
PMCPMC7738244

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