Evidence map›Paper›PMID 31636335›Full record

ArticleScientific reports2019

A micropatterned substrate for on-surface enzymatic labelling of linearized long DNA molecules.

Dharma Varapula, Eric LaBouff, Kaitlin Raseley, Lahari Uppuluri, Garth D Ehrlich, Moses Noh, Ming Xiao

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 37% of its field
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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. DNA Manipulation and Single-Molecule Imaging.Molecules (Basel, Switzerland) · 2021
    Review
  3. 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

7 authors at 1 institution in 1 country.

Dharma VarapulaSchool of Biomedical Engineering, Drexel University, Philadelphia, PA, 19104, USA.
Eric LaBouffSchool of Biomedical Engineering, Drexel University, Philadelphia, PA, 19104, USA.
Kaitlin RaseleySchool of Biomedical Engineering, Drexel University, Philadelphia, PA, 19104, USA.
Lahari UppuluriDepartment of Mechanical Engineering and Mechanics, Drexel University, Philadelphia, PA, 19104, USA.
Garth D EhrlichDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA, 19102, USA.ORCID http://orcid.org/0000-0003-0341-8771
Moses NohDepartment of Mechanical Engineering and Mechanics, Drexel University, Philadelphia, PA, 19104, USA.
Ming XiaoSchool of Biomedical Engineering, Drexel University, Philadelphia, PA, 19104, USA. ming.xiao@drexel.edu.
Drexel University · US

Funding

MOLECULAR ANALYSIS OF PATHOGENS IN OTITIS MEDIA BY PCRR01DC002148 · NIDCD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI EHRLICH, GARTH D. · 1994 to 2017
$6.5M
Single molecule DNA mapping for genome and CNV analysisR01HG005946 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KWOK, PUI-YAN, XIAO, MING · 2010 to 2021
$6.5M
High throughput single molecule approaches for phased genome sequence assemblyR56HG005946 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KWOK, PUI-YAN, XIAO, MING · 2018 to 2018
$344k
NHGRI NIH HHS R01 HG005946NHGRI NIH HHS R56 HG005946NIDCD NIH HHS R01 DC002148
6 · The paper itself

Abstract

Optical mapping of linearized DNA molecules is a promising new technology for sequence assembly and scaffolding, large structural variant detection, and diagnostics. This is currently achieved either using nanochannel confinement or by stretching single DNA molecules on a solid surface. While the first method necessitates DNA labelling before linearization, the latter allows for modification post-linearization, thereby affording increased process flexibility. Each method is constrained by various physical and chemical limitations. One of the most common techniques for linearization of DNA uses a hydrophobic surface and a receding meniscus, termed molecular combing. Here, we report the development of a microfabricated surface that can not only comb the DNA molecules efficiently but also provides for sequence-specific enzymatic fluorescent DNA labelling. By modifying a glass surface with two contrasting functionalities, such that DNA binds selectively to one of the two regions, we can control DNA extension, which is known to be critical for sequence-recognition by an enzyme. Moreover, the surface modification provides enzymatic access to the DNA backbone, as well as minimizing non-specific fluorescent dye adsorption. These enhancements make the designed surface suitable for large-scale and high-resolution single DNA molecule studies.

Indexed as

MicrotechnologyStaining and LabelingDNAFluorescenceHumansMolecular WeightPolyethylene GlycolsSubstrate SpecificitySurface PropertiesDNAPolyethylene Glycols

Identifiers

PMID31636335
PMCPMC6803683
OpenAlexW2981036624

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.