Evidence map›Paper›PMID 35168570›Full record

ArticleBMC genomics2022

MutationalPatterns: the one stop shop for the analysis of mutational processes.

Freek Manders, Arianne M Brandsma, Jurrian de Kanter, Mark Verheul, Rurika Oka, Markus J van Roosmalen, Bastiaan van der Roest, Arne van Hoeck, Edwin Cuppen, Ruben van Boxtel

Abstract read
In one paragraph

Article in BMC genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 127 papers.

0numbers the graph read from it
0cells of the map it votes in
127citing papers in PubMed
–field-weighted citation impact
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

127 citing papers in PubMed.

  1. Patritumab deruxtecan in HRNature medicine · 2025
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  8. Integrated Multiomic Profiling Enhances Risk Stratification and Prognostication in Canine Osteosarcoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
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67 more citing papers are in PubMed but not listed here.

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

10 authors.

Freek MandersPrincess Máxima Center for Pediatric Oncology, Heidelberglaan 25, 3584CS, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0001-6197-347X
Arianne M BrandsmaPrincess Máxima Center for Pediatric Oncology, Heidelberglaan 25, 3584CS, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-7969-4046
Jurrian de KanterPrincess Máxima Center for Pediatric Oncology, Heidelberglaan 25, 3584CS, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0001-5665-3711
Mark VerheulPrincess Máxima Center for Pediatric Oncology, Heidelberglaan 25, 3584CS, Utrecht, The Netherlands.
Rurika OkaPrincess Máxima Center for Pediatric Oncology, Heidelberglaan 25, 3584CS, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0003-4107-7250
Markus J van RoosmalenPrincess Máxima Center for Pediatric Oncology, Heidelberglaan 25, 3584CS, Utrecht, The Netherlands.
Bastiaan van der RoestOncode Institute, Jaarbeursplein 6, 3521 AL, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-8985-8964
Arne van HoeckOncode Institute, Jaarbeursplein 6, 3521 AL, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-6570-1452
Edwin CuppenOncode Institute, Jaarbeursplein 6, 3521 AL, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-0400-9542
Ruben van BoxtelPrincess Máxima Center for Pediatric Oncology, Heidelberglaan 25, 3584CS, Utrecht, The Netherlands. R.vanBoxtel@prinsesmaximacentrum.nl.ORCID http://orcid.org/0000-0003-1285-2836

Funding

Nederlandse Organisatie voor Wetenschappelijk Onderzoek 016.Vidi.171.023
6 · The paper itself

Abstract

backgroundThe collective of somatic mutations in a genome represents a record of mutational processes that have been operative in a cell. These processes can be investigated by extracting relevant mutational patterns from sequencing data.

resultsHere, we present the next version of MutationalPatterns, an R/Bioconductor package, which allows in-depth mutational analysis of catalogues of single and double base substitutions as well as small insertions and deletions. Major features of the package include the possibility to perform regional mutation spectra analyses and the possibility to detect strand asymmetry phenomena, such as lesion segregation. On top of this, the package also contains functions to determine how likely it is that a signature can cause damaging mutations (i.e., mutations that affect protein function). This updated package supports stricter signature refitting on known signatures in order to prevent overfitting. Using simulated mutation matrices containing varied signature contributions, we showed that reliable refitting can be achieved even when only 50 mutations are present per signature. Additionally, we incorporated bootstrapped signature refitting to assess the robustness of the signature analyses. Finally, we applied the package on genome mutation data of cell lines in which we deleted specific DNA repair processes and on large cancer datasets, to show how the package can be used to generate novel biological insights.

conclusionsThis novel version of MutationalPatterns allows for more comprehensive analyses and visualization of mutational patterns in order to study the underlying processes. Ultimately, in-depth mutational analyses may contribute to improved biological insights in mechanisms of mutation accumulation as well as aid cancer diagnostics. MutationalPatterns is freely available at http://bioconductor.org/packages/MutationalPatterns .

Indexed as

Genome, HumanNeoplasmsDNA Mutational AnalysisDNA RepairHumansMutationMutation AccumulationBase substitutionsIndelsMutagenic processesMutational signaturesRRegional mutation patternsSomatic mutations

Identifiers

PMID35168570
PMCPMC8845394

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.