Evidence map›Paper›PMID 30367503›Full record

ArticleElectrophoresis2019

Development of 3D printed mesofluidic devices to elute and concentrate DNA.

Cody Masters, Jocelyn Dolphin, April Maschmann, Keegan McGill, Matthew Moore, Drew Thompson, Kristy L Kounovsky-Shafer

Abstract read
In one paragraph

Article in Electrophoresis, 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
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  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.

Cody MastersDepartment of Chemistry, University of Nebraska - Kearney, Kearney, NE, 68849, USA.
Jocelyn DolphinDepartment of Chemistry, University of Nebraska - Kearney, Kearney, NE, 68849, USA.
April MaschmannDepartment of Chemistry, University of Nebraska - Kearney, Kearney, NE, 68849, USA.
Keegan McGillDepartment of Chemistry, University of Nebraska - Kearney, Kearney, NE, 68849, USA.
Matthew MooreDepartment of Chemistry, University of Nebraska - Kearney, Kearney, NE, 68849, USA.
Drew ThompsonDepartment of Chemistry, University of Nebraska - Kearney, Kearney, NE, 68849, USA.
Kristy L Kounovsky-ShaferDepartment of Chemistry, University of Nebraska - Kearney, Kearney, NE, 68849, USA.ORCID 0000-0002-0544-962X

Funding

UNMC Structural Biology CoreP20GM103427 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Heather Colleen Jensen-Smith · 2012 to 2026
$59.2M
National Institute for General Medical Science 5605100122001NIGMS NIH HHS P20 GM103427University of Nebraska
6 · The paper itself

Abstract

To understand structural variation for personal genomics, an extensive ensemble of large DNA molecules will be required to span large structural variations. Nanocoding, a whole-genome analysis platform, can analyze large DNA molecules for the construction of physical restriction maps of entire genomes. However, handling of large DNA is difficult and a system is needed to concentrate large DNA molecules, while keeping the molecules intact. Insert technology was developed to protect large DNA molecules during routine cell lysis and molecular biology techniques. However, eluting and concentrating DNA molecules has been difficult in the past. Utilizing 3D printed mesofluidic device, a proof of principle system was developed to elute and concentrate lambda DNA molecules at the interface between a solution and a poly-acrylamide roadblock. The matrix allowed buffer solution to move through the pores in the matrix; however, it slowed down the progression of DNA in the matrix, since the molecules were so large and the pore size was small. Using fluorescence intensity of the insert, 84% of DNA was eluted from the insert and 45% of DNA was recovered in solution from the eluted DNA. DNA recovered was digested with a restriction enzyme to determine that the DNA molecules remained full length during the elution and concentration of DNA.

Indexed as

Printing, Three-DimensionalAcrylic ResinsDNAEquipment DesignFluorescent DyesMicrofluidic Analytical TechniquesPolymerizationAcrylic ResinsDNAFluorescent Dyespolyacrylamide gels3D printingDNA concentration deviceDNA elution

Identifiers

PMID30367503
PMCPMC12980306

What OpenQuestion holds

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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.