RNA-seq-derived sequence variations are excellent features for cell line identification

Cell lines are indispensable models for analyzing molecular mechanisms underlying human diseases. However, incorrect annotation and cross-contamination can introduce severe bias in respective studies. Accordingly, various publishers request authentication of cell lines before publication. Short tandem repeat profiling is commonly used to verify cell line identity and purity but does not guarantee that published results are based on the samples tested by this method. In this study, we demonstrate that RNA-seq-derived sequence variation information is eligible for unambiguous cell line-specific clustering. Based on this finding, we propose methods for reliable cell line identification from RNA-seq data using supervised machine learning methods. In addition, we demonstrate the ability to detect cross-contamination of human cell lines. The presented methods are insensitive to different data pre-processing steps and quality measures. The proposed topFracCCLE algorithm for cell line identification and detection of cross-contamination is available as R-script at https://github.com/HuettelmaierLab/topFracCCLE.

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Publication Details

Journal
Computational and Structural Biotechnology Journal
Published
2025-01-01
DOI
https://doi.org/10.1016/j.csbj.2025.10.039
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
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article

RNA-seq-derived sequence variations are excellent features for cell line identification

Alice Wedler, Markus Glaß, Frank Hause, Lisa Müller et al.
Computational and Structural Biotechnology Journal
Single-cell and spatial transcriptomics
article

RNA-seq-derived sequence variations are excellent features for cell line identification

Alice Wedler, Markus Glaß, Frank Hause, Lisa Müller, Sven Hagemann, Danny Misiak, Tony Gutschner, Stefan Hüttelmaier, Simon Müller, Claudia Misiak, Khursheed Ul Islam Mir, Jana Lange
article en

Abstract

Cell lines are indispensable models for analyzing molecular mechanisms underlying human diseases. However, incorrect annotation and cross-contamination can introduce severe bias in respective studies. Accordingly, various publishers request authentication of cell lines before publication. Short tandem repeat profiling is commonly used to verify cell line identity and purity but does not guarantee that published results are based on the samples tested by this method. In this study, we demonstrate that RNA-seq-derived sequence variation information is eligible for unambiguous cell line-specific clustering. Based on this finding, we propose methods for reliable cell line identification from RNA-seq data using supervised machine learning methods. In addition, we demonstrate the ability to detect cross-contamination of human cell lines. The presented methods are insensitive to different data pre-processing steps and quality measures. The proposed topFracCCLE algorithm for cell line identification and detection of cross-contamination is available as R-script at https://github.com/HuettelmaierLab/topFracCCLE.

Computational and Structural Biotechnology JournalVol. 27
New York Genome Center (US), Martin Luther University Halle-Wittenberg (DE)
Openalex Percentile: Top 72%
Single-cell and spatial transcriptomics
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