Evidence map›Paper›PMID 26221198›Full record

ArticleBiomicrofluidics2015

DNA-library assembly programmed by on-demand nano-liter droplets from a custom microfluidic chip.

Uwe Tangen, Gabriel Antonio S Minero, Abhishek Sharma, Patrick F Wagler, Rafael Cohen, Ofir Raz, Tzipy Marx, Tuval Ben-Yehezkel, John S McCaskill

Open access · bronzeAbstract read
In one paragraph

Article in Biomicrofluidics, 2015. 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
1.6field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Protein design-scapes generated by microfluidic DNA assembly elucidate domain coupling in the bacterial histidine kinase CpxA.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  4. Article
  5. Review
  6. Article
  7. 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

9 authors at 2 institutions in 2 countries.

Uwe TangenFaculty of Chemistry and Biochemistry, Microsystems Chemistry and BioIT (BioMIP), Ruhr-University Bochum , 44780 Bochum, Germany.
Gabriel Antonio S MineroFaculty of Chemistry and Biochemistry, Microsystems Chemistry and BioIT (BioMIP), Ruhr-University Bochum , 44780 Bochum, Germany.
Abhishek SharmaFaculty of Chemistry and Biochemistry, Microsystems Chemistry and BioIT (BioMIP), Ruhr-University Bochum , 44780 Bochum, Germany.
Patrick F WaglerFaculty of Chemistry and Biochemistry, Microsystems Chemistry and BioIT (BioMIP), Ruhr-University Bochum , 44780 Bochum, Germany.
Rafael CohenDepartment of Biological Chemistry, Weizmann Institute of Science , Rehovot, Israel.
Ofir RazDepartment of Biological Chemistry, Weizmann Institute of Science , Rehovot, Israel.
Tzipy MarxDepartment of Biological Chemistry, Weizmann Institute of Science , Rehovot, Israel.
Tuval Ben-YehezkelDepartment of Biological Chemistry, Weizmann Institute of Science , Rehovot, Israel.
John S McCaskillFaculty of Chemistry and Biochemistry, Microsystems Chemistry and BioIT (BioMIP), Ruhr-University Bochum , 44780 Bochum, Germany.
Ruhr University Bochum · DEWeizmann Institute of Science · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanoscale synthetic biology can benefit from programmable nanoliter-scale processing of DNA in microfluidic chips if they are interfaced effectively to biochemical arrays such as microwell plates. Whereas active microvalve chips require complex fabrication and operation, we show here how a passive and readily fabricated microchip can be employed for customizable nanoliter scale pipetting and reaction control involving DNA. This recently developed passive microfluidic device, supporting nanoliter scale combinatorial droplet generation and mixing, is here used to generate a DNA test library with one member per droplet exported to addressed locations on microwell plates. Standard DNA assembly techniques, such as Gibson assembly, compatible with isothermal on-chip operation, are employed and checked using off-chip PCR and assembly PCR. The control of output droplet sequences and mixing performance was verified using dyes and fluorescently labeled DNA solutions, both on-chip and in external capillary channels. Gel electrophoresis of products and DNA sequencing were employed to further verify controlled combination and functional enzymatic assembly. The scalability of the results to larger DNA libraries is also addressed by combinatorial input expansion using sequential injection plugs from a multiwell plate. Hence, the paper establishes a proof of principle of the production of functional combinatorial mixtures at the nanoliter scale for one sequence per well DNA libraries.

Identifiers

PMID26221198
PMCPMC4499045
OpenAlexW1581312471

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.