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ApE, A Plasmid Editor: A Freely Available DNA Manipulation and Visualization Program
A plasmid Editor (ApE) is a free, multi-platform application for visualizing, designing, and presenting biologically relevant DNA sequences. ApE provides a flexible framework for annotating a sequence manually or using a user-defined library of features. ApE can be used in designing plasmids and oth...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580900/ https://www.ncbi.nlm.nih.gov/pubmed/36304290 http://dx.doi.org/10.3389/fbinf.2022.818619 |
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author | Davis, M. Wayne Jorgensen, Erik M. |
author_facet | Davis, M. Wayne Jorgensen, Erik M. |
author_sort | Davis, M. Wayne |
collection | PubMed |
description | A plasmid Editor (ApE) is a free, multi-platform application for visualizing, designing, and presenting biologically relevant DNA sequences. ApE provides a flexible framework for annotating a sequence manually or using a user-defined library of features. ApE can be used in designing plasmids and other constructs via in silico simulation of cloning methods such as PCR, Gibson assembly, restriction-ligation assembly and Golden Gate assembly. In addition, ApE provides a platform for creating visually appealing linear and circular plasmid maps. It is available for Mac, PC, and Linux-based platforms and can be downloaded at https://jorgensen.biology.utah.edu/wayned/ape/. |
format | Online Article Text |
id | pubmed-9580900 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95809002022-10-26 ApE, A Plasmid Editor: A Freely Available DNA Manipulation and Visualization Program Davis, M. Wayne Jorgensen, Erik M. Front Bioinform Bioinformatics A plasmid Editor (ApE) is a free, multi-platform application for visualizing, designing, and presenting biologically relevant DNA sequences. ApE provides a flexible framework for annotating a sequence manually or using a user-defined library of features. ApE can be used in designing plasmids and other constructs via in silico simulation of cloning methods such as PCR, Gibson assembly, restriction-ligation assembly and Golden Gate assembly. In addition, ApE provides a platform for creating visually appealing linear and circular plasmid maps. It is available for Mac, PC, and Linux-based platforms and can be downloaded at https://jorgensen.biology.utah.edu/wayned/ape/. Frontiers Media S.A. 2022-02-04 /pmc/articles/PMC9580900/ /pubmed/36304290 http://dx.doi.org/10.3389/fbinf.2022.818619 Text en Copyright © 2022 Davis and Jorgensen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioinformatics Davis, M. Wayne Jorgensen, Erik M. ApE, A Plasmid Editor: A Freely Available DNA Manipulation and Visualization Program |
title | ApE, A Plasmid Editor: A Freely Available DNA Manipulation and Visualization Program |
title_full | ApE, A Plasmid Editor: A Freely Available DNA Manipulation and Visualization Program |
title_fullStr | ApE, A Plasmid Editor: A Freely Available DNA Manipulation and Visualization Program |
title_full_unstemmed | ApE, A Plasmid Editor: A Freely Available DNA Manipulation and Visualization Program |
title_short | ApE, A Plasmid Editor: A Freely Available DNA Manipulation and Visualization Program |
title_sort | ape, a plasmid editor: a freely available dna manipulation and visualization program |
topic | Bioinformatics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9580900/ https://www.ncbi.nlm.nih.gov/pubmed/36304290 http://dx.doi.org/10.3389/fbinf.2022.818619 |
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