Genome Visualization

Proksee

Proksee (Paul Stothard, Univ. Alberta, Canada) - is an updated version of my go-to program for analysis and visualization of bacterial and phage genomes - CGView Server. This version includes integrated genome annotation tools and a new CGView engine written in JavaScript that allows for rapid zooming to the DNA sequence level. Extensive options are available for customizing maps and highlighting features of interest. (Instructions)


PlasMapper 3.0

PlasMapper 3.0 - allows users to generate, edit, annotate and interactively visualize publication quality plasmid maps. Additionally, it offers an option of automated codon optimization and BLAST sequence alignment.
(Reference: Wishart DS et al. 2023. Nucleic Acids Res 51(W1): W459-W467).


JPGV

Jena Prokaryotic Genome Viewer (JPGV) - from a GenBank flatfile (*.gbk) generates linear or circular plots; including if desired GC content, GC skew, purine excess and keto excess can be displayed. Also allows BLAST analysis against related genomes. Requires free registration.


GenomeVx

GenomeVx - makes editable, publication-quality, maps of mitochondrial and chloroplast genomes and of large plasmids. These maps show the location of genes and chromosomal features as well as a position scale. The program takes as input either raw feature positions or GenBank records. In the latter case, features are automatically extracted and colored. Output is in the Adobe Portable Document Format (PDF) and can be edited by programs such as Adobe Illustrator.
(Reference: G. Conant & K. Woolfe. 2008. Bioinformatics 24:861-862).


myGenomeBrowser

myGenomeBrowser - is a web-based environment that provides biologists with a way to build, query and share their genome browsers. This tool, that builds on JBrowse, is designed to give users more autonomy while simplifying and minimizing intervention from system administrators. They have extended genome browser basic features to allow users to query, analyze and share their data.
(Reference: S. Carrere & J. Gouzy. Bioinformatics (2017) 33 (8): 1255-1257).


OrganellarGenomeDRAW

OrganellarGenomeDRAW - is a suite of software tools that enable users to create high-quality visualrepresentations of both circular and linear annotated genome sequences provided as GenBank files oraccession numbers. Although all types of DNA sequences are accepted as input, the software has beenspecifically optimized to properly depict features of organellar genomes. A recent extension facilitates theplotting of quantitative gene expression data, such as transcript or protein abundance data, directly ontothe genome map
(Reference:Lohse M, et al. 2013. Nucleic Acids Res. 41(Web Server issue):W575-81).


PlasmaDNA

PlasmaDNA - Starting with a primary DNA sequence, PlasmaDNA looks for restriction sites, open reading frames, primer annealing sequences, and various common domains. The databases are easily expandable by the user to fit his most common cloning needs. PlasmaDNA can manage and graphically represent multiple sequences at the same time, and keeps in memory the overhangs at the end of the sequences if any. This means that it is possible to virtually digest fragments, to add the digestion products to the project, and to ligate together fragments with compatible ends to generate the new sequences. Excellent package for plasmids.
(Reference: Angers-Loustau A et al. 2007. BMC Mol Biol. 2007; 8:77).


GECA

GECA - is a user-friendly tool for representing gene exon/intron organization and highlighting changes in gene structure among members of a gene family. It relies on protein alignment, completed with the identification of common introns in the corresponding genes using CIWOG. GECA produces a main graphical representation showing the resulting aligned set of gene structures, where exons are to scale. The important and original feature of GECA is that it combines these gene structures with a symbolic display highlighting sequence similarity between subsequent genes. It is worth noting that this combination of gene structure with the indications of similarities between related genes allows rapid identification of possible events of gain or loss of introns, or points to erroneous structural annotations. The output image is generated in a portable network graphics format which can be used for scientific publications.
(Reference: Fawal N, et al. 2012. Bioinformatics; 28:1398-9).

Updated: December, 2025