Benchmark and Parameter Sensitivity Analysis of Single-Cell RNA Sequencing Clustering Methods
Single-cell RNA-seq (scRNAseq) is a powerful tool to study heterogeneity of cells. Recently, several clustering based methods have been proposed to identify distinct cell populations. These methods are based on different statistical models and usually require to perform several additional steps, suc...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2019-12-01
|
Series: | Frontiers in Genetics |
Subjects: | |
Online Access: | https://www.frontiersin.org/article/10.3389/fgene.2019.01253/full |
_version_ | 1818007811050700800 |
---|---|
author | Monika Krzak Yordan Raykov Alexis Boukouvalas Luisa Cutillo Claudia Angelini |
author_facet | Monika Krzak Yordan Raykov Alexis Boukouvalas Luisa Cutillo Claudia Angelini |
author_sort | Monika Krzak |
collection | DOAJ |
description | Single-cell RNA-seq (scRNAseq) is a powerful tool to study heterogeneity of cells. Recently, several clustering based methods have been proposed to identify distinct cell populations. These methods are based on different statistical models and usually require to perform several additional steps, such as preprocessing or dimension reduction, before applying the clustering algorithm. Individual steps are often controlled by method-specific parameters, permitting the method to be used in different modes on the same datasets, depending on the user choices. The large number of possibilities that these methods provide can intimidate non-expert users, since the available choices are not always clearly documented. In addition, to date, no large studies have invistigated the role and the impact that these choices can have in different experimental contexts. This work aims to provide new insights into the advantages and drawbacks of scRNAseq clustering methods and describe the ranges of possibilities that are offered to users. In particular, we provide an extensive evaluation of several methods with respect to different modes of usage and parameter settings by applying them to real and simulated datasets that vary in terms of dimensionality, number of cell populations or levels of noise. Remarkably, the results presented here show that great variability in the performance of the models is strongly attributed to the choice of the user-specific parameter settings. We describe several tendencies in the performance attributed to their modes of usage and different types of datasets, and identify which methods are strongly affected by data dimensionality in terms of computational time. Finally, we highlight some open challenges in scRNAseq data clustering, such as those related to the identification of the number of clusters. |
first_indexed | 2024-04-14T05:20:38Z |
format | Article |
id | doaj.art-9f33f15e483843319c6adfa621fcc443 |
institution | Directory Open Access Journal |
issn | 1664-8021 |
language | English |
last_indexed | 2024-04-14T05:20:38Z |
publishDate | 2019-12-01 |
publisher | Frontiers Media S.A. |
record_format | Article |
series | Frontiers in Genetics |
spelling | doaj.art-9f33f15e483843319c6adfa621fcc4432022-12-22T02:10:12ZengFrontiers Media S.A.Frontiers in Genetics1664-80212019-12-011010.3389/fgene.2019.01253486077Benchmark and Parameter Sensitivity Analysis of Single-Cell RNA Sequencing Clustering MethodsMonika Krzak0Yordan Raykov1Alexis Boukouvalas2Luisa Cutillo3Claudia Angelini4Institute for Applied Mathematics “Mauro Picone”, Naples, ItalyDepartment of Mathematics, Aston University, Birmingham, United KingdomMachine Learning Engineer Team, Prowler.io, Cambridge, United KingdomSchool of Mathematics, University of Leeds, Leeds, United KingdomInstitute for Applied Mathematics “Mauro Picone”, Naples, ItalySingle-cell RNA-seq (scRNAseq) is a powerful tool to study heterogeneity of cells. Recently, several clustering based methods have been proposed to identify distinct cell populations. These methods are based on different statistical models and usually require to perform several additional steps, such as preprocessing or dimension reduction, before applying the clustering algorithm. Individual steps are often controlled by method-specific parameters, permitting the method to be used in different modes on the same datasets, depending on the user choices. The large number of possibilities that these methods provide can intimidate non-expert users, since the available choices are not always clearly documented. In addition, to date, no large studies have invistigated the role and the impact that these choices can have in different experimental contexts. This work aims to provide new insights into the advantages and drawbacks of scRNAseq clustering methods and describe the ranges of possibilities that are offered to users. In particular, we provide an extensive evaluation of several methods with respect to different modes of usage and parameter settings by applying them to real and simulated datasets that vary in terms of dimensionality, number of cell populations or levels of noise. Remarkably, the results presented here show that great variability in the performance of the models is strongly attributed to the choice of the user-specific parameter settings. We describe several tendencies in the performance attributed to their modes of usage and different types of datasets, and identify which methods are strongly affected by data dimensionality in terms of computational time. Finally, we highlight some open challenges in scRNAseq data clustering, such as those related to the identification of the number of clusters.https://www.frontiersin.org/article/10.3389/fgene.2019.01253/fullsingle-cell RNA-seqclustering methodsbenchmarkparameter sensitivity analysishigh-dimensional data analysis |
spellingShingle | Monika Krzak Yordan Raykov Alexis Boukouvalas Luisa Cutillo Claudia Angelini Benchmark and Parameter Sensitivity Analysis of Single-Cell RNA Sequencing Clustering Methods Frontiers in Genetics single-cell RNA-seq clustering methods benchmark parameter sensitivity analysis high-dimensional data analysis |
title | Benchmark and Parameter Sensitivity Analysis of Single-Cell RNA Sequencing Clustering Methods |
title_full | Benchmark and Parameter Sensitivity Analysis of Single-Cell RNA Sequencing Clustering Methods |
title_fullStr | Benchmark and Parameter Sensitivity Analysis of Single-Cell RNA Sequencing Clustering Methods |
title_full_unstemmed | Benchmark and Parameter Sensitivity Analysis of Single-Cell RNA Sequencing Clustering Methods |
title_short | Benchmark and Parameter Sensitivity Analysis of Single-Cell RNA Sequencing Clustering Methods |
title_sort | benchmark and parameter sensitivity analysis of single cell rna sequencing clustering methods |
topic | single-cell RNA-seq clustering methods benchmark parameter sensitivity analysis high-dimensional data analysis |
url | https://www.frontiersin.org/article/10.3389/fgene.2019.01253/full |
work_keys_str_mv | AT monikakrzak benchmarkandparametersensitivityanalysisofsinglecellrnasequencingclusteringmethods AT yordanraykov benchmarkandparametersensitivityanalysisofsinglecellrnasequencingclusteringmethods AT alexisboukouvalas benchmarkandparametersensitivityanalysisofsinglecellrnasequencingclusteringmethods AT luisacutillo benchmarkandparametersensitivityanalysisofsinglecellrnasequencingclusteringmethods AT claudiaangelini benchmarkandparametersensitivityanalysisofsinglecellrnasequencingclusteringmethods |