Evidence map›Paper›PMID 41542088›Full record

ArticleComputational and structural biotechnology journal2025

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

Lisa Müller, Simon Müller, Khursheed Ul Islam Mir, Jana Lange, Sven Hagemann, Alice Wedler, Frank Hause, Claudia Misiak, Danny Misiak, Tony Gutschner and 2 more

Abstract read
In one paragraph

Article in Computational and structural biotechnology journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Lisa MüllerInstitute of Molecular Medicine, Section for RNA Biology and Pathogenesis, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Straße 3a, 06120, Halle, Germany.
Simon MüllerNew York Genome Center, Department of Biology, New York University, 101 Avenue of the Americas, 10013, New York, United States.
Khursheed Ul Islam MirInstitute of Molecular Medicine, Section for Molecular Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Straße 3a, 06120, Halle, Germany.
Jana LangeInstitute of Molecular Medicine, Section for Molecular Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Straße 3a, 06120, Halle, Germany.
Sven HagemannInstitute of Molecular Medicine, Section for Molecular Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Straße 3a, 06120, Halle, Germany.
Alice WedlerInstitute of Molecular Medicine, Section for Molecular Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Straße 3a, 06120, Halle, Germany.
Frank HauseInstitute of Molecular Medicine, Section for Molecular Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Straße 3a, 06120, Halle, Germany.
Claudia MisiakInstitute of Molecular Medicine, Section for Molecular Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Straße 3a, 06120, Halle, Germany.
Danny MisiakInstitute of Molecular Medicine, Section for Molecular Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Straße 3a, 06120, Halle, Germany.
Tony GutschnerInstitute of Molecular Medicine, Section for RNA Biology and Pathogenesis, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Straße 3a, 06120, Halle, Germany.
Stefan HüttelmaierInstitute of Molecular Medicine, Section for Molecular Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Straße 3a, 06120, Halle, Germany.
Markus GlaßInstitute of Molecular Medicine, Section for Molecular Cell Biology, Faculty of Medicine, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Straße 3a, 06120, Halle, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

CCLECell line identificationCross-contaminationK-nearest neighborMachine learning

Identifiers

PMID41542088
PMCPMC12800365

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.