Easily preview your created DNA maps and analyzing enzymes

SnapGene Viewer

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SnapGene Viewer 8.0.0

  -  124.01 MB  -  Demo
Free Download

Security Status

  • Latest Version

    SnapGene Viewer 8.0.1

  • Operating System

    Windows 7 / Windows 7 64 / Windows 8 / Windows 8 64 / Windows 10 / Windows 10 64

  • User Rating

    Click to vote

  • Author / Product

    GSL Biotech LLC / External Link

  • Filename

    snapgene_8.0.0_win.exe

  • MD5 Checksum

    27c9ebd14342bbd0a8f6da1cedbcd576

Sometimes latest versions of the software can cause issues when installed on older devices or devices running an older version of the operating system.

Software makers usually fix these issues but it can take them some time. What you can do in the meantime is to download and install an older version of SnapGene Viewer 8.0.0.


For those interested in downloading the most recent release of SnapGene Viewer or reading our review, simply click here.


All old versions distributed on our website are completely virus-free and available for download at no cost.


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If you have any questions or ideas that you want to share with us - head over to our Contact page and let us know. We value your feedback!

Download SnapGene Viewer 8.0.0

What's new in this version:

- SnapGene 8.0 brings a fresh look and feel to the main data viewers, with new capabilities for bulk annotation and data manipulation, and new ways to edit alignments to a reference sequence.

Bulk annotate your plasmids with features and primers:
- Quickly detect common features and add primers from a list onto multiple sequences selected in the Project folder panel, change sequence attributes like methylation and topology and easily perform alignments and gel simulations on selected sequences.

Modern, streamlined Map, Sequence, Features and Primers views:
- Refreshed Map, Sequence, Features and Primers views are restructured and simplified to highlight key data and capabilities, with flexible filtering and sorting added to Features and Primers tables.

Edit Alignments to a Reference DNA Sequence:
- You can now validate your sequences with confidence by editing the gap positions in your Sanger traces and virtual constructs when using Align to a Reference DNA Sequence

Enhancements to File and Folder Interactions:
- Data management is streamlined with improved file selection in the folder panel and new visualization and manipulation of unsaved files

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