Evidence map›Paper›PMID 30768372›Full record

ArticleSLAS technology2019

Standardizing Automated DNA Assembly: Best Practices, Metrics, and Protocols Using Robots.

David I Walsh, Marilene Pavan, Luis Ortiz, Scott Wick, Johanna Bobrow, Nicholas J Guido, Sarah Leinicke, Dany Fu, Shreya Pandit, Lucy Qin and 2 more

Abstract read
In one paragraph

Article in SLAS technology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Self-documenting plasmids.Trends in biotechnology · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Setting Up an Automated Biomanufacturing Laboratory.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  14. Biological Materials: The Next Frontier for Cell-Free Synthetic Biology.Frontiers in bioengineering and biotechnology · 2020
    Review
  15. Article
  16. 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

12 authors.

David I Walsh1 Bioengineering Systems and Technologies, MIT Lincoln Laboratory, Lexington, MA, USA.
Marilene Pavan3 Biological Design Center, Boston University, Boston, MA, USA.
Luis Ortiz3 Biological Design Center, Boston University, Boston, MA, USA.
Scott Wick1 Bioengineering Systems and Technologies, MIT Lincoln Laboratory, Lexington, MA, USA.
Johanna Bobrow1 Bioengineering Systems and Technologies, MIT Lincoln Laboratory, Lexington, MA, USA.
Nicholas J Guido1 Bioengineering Systems and Technologies, MIT Lincoln Laboratory, Lexington, MA, USA.
Sarah Leinicke6 Hariri Institute for Computing, Boston University, Boston, MA, USA.
Dany Fu6 Hariri Institute for Computing, Boston University, Boston, MA, USA.
Shreya Pandit6 Hariri Institute for Computing, Boston University, Boston, MA, USA.
Lucy Qin6 Hariri Institute for Computing, Boston University, Boston, MA, USA.
Peter A Carr1 Bioengineering Systems and Technologies, MIT Lincoln Laboratory, Lexington, MA, USA.
Douglas Densmore3 Biological Design Center, Boston University, Boston, MA, USA.

Funding

MIT Center for Integrative Synthetic BiologyP50GM098792 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI WEISS, RON · 2013 to 2017
$11.0M
ANIMAL HUSBANDRY SUPPORT SERVICES FOR NIEHS27304C0002 · NIEHS · 2007 to 2008
$5.0M
Genetic circuits for high-throughput, multi-sensory, live cell microRNA profR01CA173712 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI WEISS, RON · 2013 to 2017
$2.5M
Role of Mitochondrial CYP2E1 in Chemical Exposure-Driven NeurodegenerationF32ES027306 · NIEHS · DUKE UNIVERSITY · PI HARTMAN, JESSICA HELENE · 2016 to 2018
$171k
Investigation of metabolites related to manganese exposureF31ES027304 · NIEHS · UNIVERSITY OF WASHINGTON · PI BAKER, MARISSA GAYL · 2016 to 2017
$61k
NCI NIH HHS R01 CA173712NIEHS NIH HHS 27304C0002NIEHS NIH HHS 27306C0002NIGMS NIH HHS P50 GM098792
6 · The paper itself

Abstract

The advancement of synthetic biology requires the ability to create new DNA sequences to produce unique behaviors in biological systems. Automation is increasingly employed to carry out well-established assembly methods of DNA fragments in a multiplexed, high-throughput fashion, allowing many different configurations to be tested simultaneously. However, metrics are required to determine when automation is warranted based on factors such as assembly methodology, protocol details, and number of samples. The goal of our synthetic biology automation work is to develop and test protocols, hardware, and software to investigate and optimize DNA assembly through quantifiable metrics. We performed a parameter analysis of DNA assembly to develop a standardized, highly efficient, and reproducible MoClo protocol, suitable to be used both manually and with liquid-handling robots. We created a key DNA assembly metric (Q-metric) to characterize a given automation method's advantages over conventional manual manipulations with regard to researchers' highest-priority parameters: output, cost, and time. A software tool called Puppeteer was developed to formally capture these metrics, help define the assembly design, and provide human and robotic liquid-handling instructions. Altogether, we contribute to a growing foundation of standardizing practices, metrics, and protocols for automating DNA assembly.

Indexed as

Practice Guidelines as TopicAutomation, LaboratoryCloning, MolecularDNAGenetic EngineeringRoboticsSynthetic BiologyDNADNA assemblyliquid-handling robotsmetricsstandardssynthetic biology

Identifiers

PMID30768372
PMCPMC6819997

What OpenQuestion holds

Textmetadata
LicenceTDM
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.