Evidence map›Paper›PMID 24681819›Full record

ArticleScientific reports2014

Non-random DNA fragmentation in next-generation sequencing.

Maria S Poptsova, Irina A Il'icheva, Dmitry Yu Nechipurenko, Larisa A Panchenko, Mingian V Khodikov, Nina Y Oparina, Robert V Polozov, Yury D Nechipurenko, Sergei L Grokhovsky

Abstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing 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

57 citing papers in PubMed.

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  10. Review
  11. Genomic analyses elucidateEcology and evolution · 2024
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  12. Core Promoter Regions of Antisense and Long Intergenic Non-Coding RNAs.International journal of molecular sciences · 2023
    Article
  13. Retinitis Pigmentosa: Current Clinical Management and Emerging Therapies.International journal of molecular sciences · 2023
    Review
  14. Article
  15. Frontiers in microbiology · 2023
    Article
  16. Article
  17. Article
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  20. Review
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

9 authors.

Maria S PoptsovaDepartment of Physics, Moscow State University, Moscow, Russia.
Irina A Il'ichevaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Dmitry Yu NechipurenkoDepartment of Physics, Moscow State University, Moscow, Russia.
Larisa A PanchenkoDepartment of Biology, Moscow State University, Moscow, Russia.
Mingian V KhodikovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Nina Y OparinaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Robert V PolozovInstitute of Theoretical and Experimental Biophysics, Russian Academy of Sciences, Puschino, Moscow Region, Russia.
Yury D Nechipurenko1] Department of Physics, Moscow State University, Moscow, Russia [2] Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Sergei L GrokhovskyEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Next Generation Sequencing (NGS) technology is based on cutting DNA into small fragments, and their massive parallel sequencing. The multiple overlapping segments termed "reads" are assembled into a contiguous sequence. To reduce sequencing errors, every genome region should be sequenced several dozen times. This sequencing approach is based on the assumption that genomic DNA breaks are random and sequence-independent. However, previously we showed that for the sonicated restriction DNA fragments the rates of double-stranded breaks depend on the nucleotide sequence. In this work we analyzed genomic reads from NGS data and discovered that fragmentation methods based on the action of the hydrodynamic forces on DNA, produce similar bias. Consideration of this non-random DNA fragmentation may allow one to unravel what factors and to what extent influence the non-uniform coverage of various genomic regions.

Identifiers

PMID24681819
PMCPMC3970190

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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.