Seurat function argument values in scRNA-seq data analysis: potential pitfalls and refinements for biological interpretation

Processing biological data is a challenge of paramount importance as the amount of accumulated data has been annually increasing along with the emergence of new methods for studying biological objects. Blind application of mathematical methods in biology may lead to erroneous hypotheses and conclusions. Here we narrow our focus down to a small set of mathematical methods applied upon standard processing of scRNA-seq data: preprocessing, dimensionality reduction, integration, and clustering (using machine learning methods for clustering). Normalization and scaling are standard manipulations for the pre-processing with LogNormalize (natural-log transformation), CLR (centered log ratio transformation), and RC (relative counts) being employed as methods for data transformation. The justification for applying these methods in biology is not discussed in methodological articles. The essential aspect of dimensionality reduction is to identify the stable patterns which are deliberately removed upon mathematical data processing as being redundant, albeit containing important minor details for biological interpretation. There are no established rules for integration of datasets obtained at different sampling times or conditions. Clustering calls for reconsidering its application specifically for biological data processing. The novelty of the present study lies in an integrated approach of biology and bioinformatics to elucidate biological insights upon data processing.

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Publication Details

Journal
Frontiers in Bioinformatics
Published
2025-02-12
DOI
https://doi.org/10.3389/fbinf.2025.1519468
Citations
7
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
5.64

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article

Seurat function argument values in scRNA-seq data analysis: potential pitfalls and refinements for biological interpretation

Е. В. Семина, Kseniya Rubina, E. V. Vasilyeva, Mikhail Arbatsky et al.
7 citations
Frontiers in Bioinformatics
Single-cell and spatial transcriptomics
5.64
article

Seurat function argument values in scRNA-seq data analysis: potential pitfalls and refinements for biological interpretation

Е. В. Семина, Kseniya Rubina, E. V. Vasilyeva, Mikhail Arbatsky, V. I. Saveliev, Veronika Sysoeva
article en
7 citations

Abstract

Processing biological data is a challenge of paramount importance as the amount of accumulated data has been annually increasing along with the emergence of new methods for studying biological objects. Blind application of mathematical methods in biology may lead to erroneous hypotheses and conclusions. Here we narrow our focus down to a small set of mathematical methods applied upon standard processing of scRNA-seq data: preprocessing, dimensionality reduction, integration, and clustering (using machine learning methods for clustering). Normalization and scaling are standard manipulations for the pre-processing with LogNormalize (natural-log transformation), CLR (centered log ratio transformation), and RC (relative counts) being employed as methods for data transformation. The justification for applying these methods in biology is not discussed in methodological articles. The essential aspect of dimensionality reduction is to identify the stable patterns which are deliberately removed upon mathematical data processing as being redundant, albeit containing important minor details for biological interpretation. There are no established rules for integration of datasets obtained at different sampling times or conditions. Clustering calls for reconsidering its application specifically for biological data processing. The novelty of the present study lies in an integrated approach of biology and bioinformatics to elucidate biological insights upon data processing.

Frontiers in BioinformaticsVol. 5
Immanuel Kant Baltic Federal University (RU), Lomonosov Moscow State University (RU)
Russian Science Foundation
Openalex Percentile: Top 4%
Single-cell and spatial transcriptomics
5.64
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