Evidence map›Paper›PMID 32246135›Full record

ArticleNature protocols2020

Full-length sequencing of circular DNA viruses and extrachromosomal circular DNA using CIDER-Seq.

Devang Mehta, Luc Cornet, Matthias Hirsch-Hoffmann, Syed Shan-E-Ali Zaidi, Hervé Vanderschuren

Erratum issuedAbstract readComparative StudyEvaluation Study
PubMed Publisher
In one paragraph

Article in Nature protocols, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
–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

47 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Full-Length Sequencing of Circular DNA Viruses Using CIDER-Seq.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Devang MehtaLaboratory of Plant Genomics, Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada. devangmehta@ualberta.ca.ORCID http://orcid.org/0000-0002-8911-1174
Luc Cornet *Plant Genetics, TERRA Teaching and Research Center, Gembloux Agro-Bio Tech, University of Liège, Gembloux, Belgium.
Matthias Hirsch-Hoffmann *University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-4802-754X
Syed Shan-E-Ali Zaidi *Plant Genetics, TERRA Teaching and Research Center, Gembloux Agro-Bio Tech, University of Liège, Gembloux, Belgium.ORCID http://orcid.org/0000-0002-2976-4624
Hervé VanderschurenPlant Genetics, TERRA Teaching and Research Center, Gembloux Agro-Bio Tech, University of Liège, Gembloux, Belgium. herve.vanderschuren@kuleuven.be.ORCID http://orcid.org/0000-0003-2102-9737

Funding

GENE EXPRESSION DURING SPERMATOGENESISF05TW004515 · FIC · TUFTS UNIVERSITY MEDFORD · PI MALI, PEKKA T · 1991 to 1992
–
6 · The paper itself

Abstract

Circular DNA is ubiquitous in nature in the form of plasmids, circular DNA viruses, and extrachromosomal circular DNA (eccDNA) in eukaryotes. Sequencing of such molecules is essential to profiling virus distributions, discovering new viruses and understanding the roles of eccDNAs in eukaryotic cells. Circular DNA enrichment sequencing (CIDER-Seq) is a technique to enrich and accurately sequence circular DNA without the need for polymerase chain reaction amplification, cloning, and computational sequence assembly. The approach is based on randomly primed circular DNA amplification, which is followed by several enzymatic DNA repair steps and then by long-read sequencing. CIDER-Seq includes a custom data analysis package (CIDER-Seq Data Analysis Software 2) that implements the DeConcat algorithm to deconcatenate the long sequencing products of random circular DNA amplification into the intact sequences of the input circular DNA. The CIDER-Seq data analysis package can generate full-length annotated virus genomes, as well as circular DNA sequences of novel viruses. Applications of CIDER-Seq also include profiling of eccDNA molecules such as transposable elements (TEs) from biological samples. The method takes ~2 weeks to complete, depending on the computational resources available. Owing to the present constraints of long-read single-molecule sequencing, the accuracy of circular virus and eccDNA sequences generated by the CIDER-Seq method scales with sequence length, and the greatest accuracy is obtained for molecules <10 kb long.

Indexed as

ArabidopsisDNA, CircularDNA, ViralNucleic Acid Amplification TechniquesSequence Analysis, DNADNA, CircularDNA, Viral

Identifiers

What OpenQuestion holds

Textmetadata
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.