Evidence map›Paper›PMID 33318186›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Direct quantification of in vivo mutagenesis and carcinogenesis using duplex sequencing.

Charles C Valentine, Robert R Young, Mark R Fielden, Rohan Kulkarni, Lindsey N Williams, Tan Li, Sheroy Minocherhomji, Jesse J Salk

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing 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

67 citing papers in PubMed.

  1. Article
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  9. Review
  10. Article
  11. Detection of mutations: from Ames test to duplex sequencing.Frontiers in molecular biosciences · 2026
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

7 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

8 authors.

Charles C ValentineTwinStrand Biosciences, Seattle, WA 98121.ORCID 0000-0001-5630-7368
Robert R YoungMilliporeSigma/BioReliance Toxicology Testing Services, Rockville, MD 20850.ORCID 0000-0002-3783-782X
Mark R FieldenAmgen Research, Amgen, Thousand Oaks, CA 91320.
Rohan KulkarniMilliporeSigma/BioReliance Toxicology Testing Services, Rockville, MD 20850.ORCID 0000-0001-5404-4170
Lindsey N WilliamsTwinStrand Biosciences, Seattle, WA 98121.ORCID 0000-0003-3757-2582
Tan LiTwinStrand Biosciences, Seattle, WA 98121.ORCID 0000-0002-4480-5674
Sheroy MinocherhomjiAmgen Research, Amgen, Thousand Oaks, CA 91320.ORCID 0000-0002-1101-4761
Jesse J SalkTwinStrand Biosciences, Seattle, WA 98121; jjsalk@twinstrandbio.com.ORCID 0000-0002-7804-0550

Funding

Development of a Genotoxicity Assay using Duplex SequencingR44ES030642 · NIEHS · TWINSTRAND BIOSCIENCES, INC. · PI SALK, JESSE J · 2019 to 2021
$1.7M
NIEHS NIH HHS R44 ES030642
6 · The paper itself

Abstract

The ability to accurately measure mutations is critical for basic research and identifying potential drug and chemical carcinogens. Current methods for in vivo quantification of mutagenesis are limited because they rely on transgenic rodent systems that are low-throughput, expensive, prolonged, and do not fully represent other species such as humans. Next-generation sequencing (NGS) is a conceptually attractive alternative for detecting mutations in the DNA of any organism; however, the limit of resolution for standard NGS is poor. Technical error rates (∼1 × 10

Indexed as

AnimalsCarcinogenesisCarcinogensCluster AnalysisDNAGenes, rasGenetic LociGenomeHigh-Throughput Nucleotide SequencingHumansMice, TransgenicMutagenesisMutationNeoplasmsOncogenesPhenotypeCarcinogensDNADNA repairerror-corrected sequencinggenetic toxicologygenotoxicitypreclinical cancer risk assessment

Identifiers

PMID33318186
PMCPMC7776782

What OpenQuestion holds

Textmetadata
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.