Evidence map›Paper›PMID 36381610›Full record

ArticleSynthetic biology (Oxford, England)2022

basicsynbio and the BASIC SEVA collection: software and vectors for an established DNA assembly method.

Matthew C Haines, Benedict Carling, James Marshall, Vasily A Shenshin, Geoff S Baldwin, Paul Freemont, Marko Storch

Open access · goldAbstract read
In one paragraph

Article in Synthetic biology (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Opportunities for engineering outer membrane vesicles using synthetic biology approaches.Extracellular vesicles and circulating nucleic acids · 2023
    Article
  6. 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 3 institutions in 1 country.

Matthew C HainesDepartment of Infectious Disease, Sir Alexander Fleming Building, South Kensington Campus, Imperial College London, London SW7 2AZ, UK.ORCID https://orcid.org/0000-0001-8493-019X
Benedict CarlingDepartment of Bioengineering, Imperial College London, London, Westminster SW7 2AZ, UK.ORCID https://orcid.org/0000-0001-7353-2444
James MarshallDepartment of Bioengineering, Imperial College London, London, Westminster SW7 2AZ, UK.ORCID https://orcid.org/0000-0002-8948-5571
Vasily A ShenshinDepartment of Life Sciences, Imperial College London, London, Westminster SW7 2AZ, UK.ORCID https://orcid.org/0000-0002-0824-6713
Geoff S BaldwinDepartment of Life Sciences, Imperial College London, London, Westminster SW7 2AZ, UK.ORCID https://orcid.org/0000-0003-4800-023X
Paul FreemontDepartment of Infectious Disease, Sir Alexander Fleming Building, South Kensington Campus, Imperial College London, London SW7 2AZ, UK.ORCID https://orcid.org/0000-0002-5658-8486
Marko StorchDepartment of Infectious Disease, Sir Alexander Fleming Building, South Kensington Campus, Imperial College London, London SW7 2AZ, UK.ORCID https://orcid.org/0000-0003-1503-8282
Imperial College London · GBLondon Biofoundry · GBHammersmith Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Standardized deoxyribonucleic acid (DNA) assembly methods utilizing modular components provide a powerful framework to explore designs and iterate through Design-Build-Test-Learn cycles. Biopart Assembly Standard for Idempotent Cloning (BASIC) DNA assembly uses modular parts and linkers, is highly accurate, easy to automate, free for academic and commercial use and enables hierarchical assemblies through an idempotent format. These features enable applications including pathway engineering, ribosome binding site (RBS) tuning, fusion protein engineering and multiplexed guide ribonucleic acid (RNA) expression. In this work, we present basicsynbio, open-source software encompassing a Web App (https://basicsynbio.web.app/) and Python Package (https://github.com/LondonBiofoundry/basicsynbio), enabling BASIC construct design via simple drag-and-drop operations or programmatically. With basicsynbio, users can access commonly used BASIC parts and linkers while designing new parts and assemblies with exception handling for common errors. Users can export sequence data and create instructions for manual or acoustic liquid-handling platforms. Instruction generation relies on the BasicBuild Open Standard, which is parsed for bespoke workflows and is serializable in JavaScript Object Notation for transfer and storage. We demonstrate basicsynbio, assembling 30 vectors using sequences including modules from the Standard European Vector Architecture (SEVA). The BASIC SEVA vector collection is compatible with BASIC and Golden Gate using BsaI. Vectors contain one of six antibiotic resistance markers and five origins of replication from different compatibility groups. The collection is available via Addgene under an OpenMTA agreement. Furthermore, vector sequences are available from within the basicsynbio application programming interface with other collections of parts and linkers, providing a powerful environment for designing assemblies for bioengineering applications.

Indexed as

bioinformaticscloningDNA assemblysynthetic biologyvectors

Identifiers

PMID36381610
PMCPMC9664905
OpenAlexW4304608986

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.