Works on: Windows 10 | Windows 8.1 | Windows 8 | Windows 7 | Windows XP | Windows 2000 | Windows 2003 | Windows 2008 | Windows Vista | Windows 2012 SHA1 Hash: 2a2fe31cc9d600c3b448b727e08cd7c6c1277b48 Size: 32.28 MB File Format: exe
Rating: 2.652173913
out of 5
based on 23 user ratings
Publisher Website: External Link Downloads: 2073 License: Free
SnapGene Viewer is a free software by GSL Biotech LLC and works on Windows 10, Windows 8.1, Windows 8, Windows 7, Windows XP, Windows 2000, Windows 2003, Windows 2008, Windows Vista, Windows 2012.
You can download SnapGene Viewer which is 32.28 MB in size and belongs to the software category Science CAD. SnapGene Viewer was released on 2016-08-09 and last updated on our database on 2017-04-14 and is currently at version 3.2.
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SnapGene Viewer Description
Working with DNA sequences can be a difficult task, even for those who are familiar with the matter. Luckily, some developers provide the necessary digital instruments for analyzing this type of data in an easier way.
Quick installation process
SnapGene Viewer has been designed as a helpful tool for biologists to handle and exchange annotated DNA sequences easier and with less effort. The application works with files as large as 1GB.
Getting the application on the system is done through an uneventful installation process that includes the option to associate specific file extensions (sequences, sequence traces and archives) with SnapGene Viewer.
User friendly interface
Due to the domain it has been built for, SnapGene is not accessible to all users. However, a single look at the interface shows that the developers did their best to come up with a layout that is intuitive and comprehensive at the same time.
As soon as a DNA file is loaded, there is a clear view of the map. There are multiple views available that allow toggling the display of enzymes on or off as well as showing the sequences, features or primers.
Features at a glance
Among the list of features available in SnapGene Viewer there is the possibility to create a DNA sequence file from punching in the sequence and export it to a GenBank format.
It sports automatic annotation of common features but it also offers the opportunity to do it manually in the case of coding sequences as well as more particular features. Primers for PCR, sequencing, or mutagenesis can be designed and annotated, too.
Conclusion
The application does not feature the functionality included in tools of the same feather, but it offers support for the most frequently used operations as far as DNA sequence analysis is concerned.