Evidence map›Paper›PMID 23894387›Full record

ArticlePloS one2013

A microfluidic DNA library preparation platform for next-generation sequencing.

Hanyoup Kim, Mais J Jebrail, Anupama Sinha, Zachary W Bent, Owen D Solberg, Kelly P Williams, Stanley A Langevin, Ronald F Renzi, James L Van De Vreugde, Robert J Meagher and 5 more

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
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  11. Printed droplet microfluidics for on demand dispensing of picoliter droplets and cells.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  12. Digital Microfluidics for Nucleic Acid Amplification.Sensors (Basel, Switzerland) · 2017
    Review
  13. Review
  14. Article
  15. Article
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  17. Review
  18. Article
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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

15 authors.

Hanyoup KimDepartment of Biotechnology and Bioengineering, Sandia National Laboratories, Livermore, California, USA.
Mais J Jebrail
Anupama Sinha
Zachary W Bent
Owen D Solberg
Kelly P Williams
Stanley A Langevin
Ronald F Renzi
James L Van De Vreugde
Robert J Meagher
Joseph S Schoeniger
Todd W Lane
Steven S Branda
Michael S Bartsch
Kamlesh D Patel

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Next-generation sequencing (NGS) is emerging as a powerful tool for elucidating genetic information for a wide range of applications. Unfortunately, the surging popularity of NGS has not yet been accompanied by an improvement in automated techniques for preparing formatted sequencing libraries. To address this challenge, we have developed a prototype microfluidic system for preparing sequencer-ready DNA libraries for analysis by Illumina sequencing. Our system combines droplet-based digital microfluidic (DMF) sample handling with peripheral modules to create a fully-integrated, sample-in library-out platform. In this report, we use our automated system to prepare NGS libraries from samples of human and bacterial genomic DNA. E. coli libraries prepared on-device from 5 ng of total DNA yielded excellent sequence coverage over the entire bacterial genome, with >99% alignment to the reference genome, even genome coverage, and good quality scores. Furthermore, we produced a de novo assembly on a previously unsequenced multi-drug resistant Klebsiella pneumoniae strain BAA-2146 (KpnNDM). The new method described here is fast, robust, scalable, and automated. Our device for library preparation will assist in the integration of NGS technology into a wide variety of laboratories, including small research laboratories and clinical laboratories.

Indexed as

Gene LibraryDNA, BacterialGenome, BacterialGenome, HumanHigh-Throughput Nucleotide SequencingHumansMicrofluidic Analytical TechniquesSequence Analysis, DNASystems IntegrationDNA, Bacterial

Identifiers

PMID23894387
PMCPMC3718812

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.