Evidence map›Paper›PMID 31226202›Full record

ArticleNucleic acids research2019

Deconvolution of nucleic-acid length distributions: a gel electrophoresis analysis tool and applications.

Riccardo Ziraldo, Massa J Shoura, Andrew Z Fire, Stephen D Levene

Abstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. DNA supercoiling-induced shapes alter minicircle hydrodynamic properties.bioRxiv : the preprint server for biology · 2023
    Article
  6. Nutrients · 2022
    Article
  7. Cell-Free DNA Fragmentation Patterns in a Cancer Cell Line.Diagnostics (Basel, Switzerland) · 2022
    Article
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

4 authors.

Riccardo ZiraldoDepartment of Bioengineering, University of Texas at Dallas, 800 W Campbell Road, Richardson, TX 75080, USA.
Massa J ShouraDepartment of Pathology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305, USA.
Andrew Z FireDepartment of Pathology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305, USA.
Stephen D LeveneDepartment of Bioengineering, University of Texas at Dallas, 800 W Campbell Road, Richardson, TX 75080, USA.

Funding

GENE REGULATION DURING EARLY DEVELOPMENT OF C. ELEGANSR01GM037706 · NIGMS · STANFORD UNIVERSITY · PI FIRE, ANDREW Z. · 1987 to 2018
$11.0M
Cellular Response to Genetic ChangeR35GM130366 · NIGMS · STANFORD UNIVERSITY · PI ANDREW Z. FIRE · 2019 to 2026
$4.8M
Single-Molecule DNA TopologyR01GM117595 · NIGMS · UNIVERSITY OF TEXAS DALLAS · PI LEVENE, STEPHEN D. · 2015 to 2018
$1.5M
NIGMS NIH HHS R01 GM037706NIGMS NIH HHS R01 GM117595NIGMS NIH HHS R35 GM130366
6 · The paper itself

Abstract

Next-generation DNA-sequencing (NGS) technologies, which are designed to streamline the acquisition of massive amounts of sequencing data, are nonetheless dependent on various preparative steps to generate DNA fragments of required concentration, purity and average size (molecular weight). Current automated electrophoresis systems for DNA- and RNA-sample quality control, such as Agilent's Bioanalyzer® and TapeStation® products, are costly to acquire and use; they also provide limited information for samples having broad size distributions. Here, we describe a software tool that helps determine the size distribution of DNA fragments in an NGS library, or other DNA sample, based on gel-electrophoretic line profiles. The software, developed as an ImageJ plug-in, allows for straightforward processing of gel images, including lane selection and fitting of univariate functions to intensity distributions. The user selects the option of fitting either discrete profiles in cases where discrete gel bands are visible or continuous profiles, having multiple bands buried under a single broad peak. The method requires only modest imaging capabilities and is a cost-effective, rigorous alternative characterization method to augment existing techniques for library quality control.

Indexed as

SoftwareAnimalsBacteriophage lambdaCaenorhabditis elegansDNADNA FragmentationElectrophoresis, Agar GelEndonucleasesGene LibraryHigh-Throughput Nucleotide SequencingHumansQuality ControlSequence Analysis, DNADNAEndonucleases

Identifiers

PMID31226202
PMCPMC6895257

What OpenQuestion holds

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LicenceCC BY-NC
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.