#Snapgene viewer author software#
There are many different open source licenses but they all must comply with the Open Source Definition - in brief: the software can be freely used, modified and shared. Programs released under this license can be used at no cost for both personal and commercial purposes.
#Snapgene viewer author code#
Open Source software is software with source code that anyone can inspect, modify or enhance. Freeware products can be used free of charge for both personal and professional (commercial use). You need to request a free trial license in order to evaluate the SnapGene app.įreeware programs can be downloaded used free of charge and without any time limitations. The open exchange of information is crucial, so SnapGene and SnapGene Viewer provide options for reading and exporting common file formats. Convert a sequence, map, or gel image to standard formats for use with other software. Export a map or simulated agarose gel to common image formats. Use the familiar, secure operating system of your computer to store and organize your Snap Gene files.Įxport a sequence to GenBank or FASTA format. It automatically records operations to create a graphical history, and stores the ancestor constructs in the final file. Use the powerful alignment tool to check whether an actual construct matches the simulated construct. If not, the translations are on separate lines. If so, the translations are linked on the same line. Use a Sequence view to see at a glance whether two translated features are in the frame. Select the fragments to be joined and their orientations, and Snap Gene will design primers. The product file stores the template and primers in its history. Use your own primers, or ask the app to design primers automatically. Highlight unique restriction sites in bold font, or choose the automatically defined Unique Cutters or Unique 6+ Cutters enzyme set. It provides elegant, information-rich windows for simulating a variety of common cloning and PCR methods. Additional features of your choosing can be added to a custom database. Annotate common features automatically, or annotate novel features manually.įind common features in your DNA sequence using SnapGene’s extensive database. When a sequence is copied and pasted, features are automatically transferred. Make insertions, deletions, replacements, and case changes. Take advantage of SnapGene’s efficient data handling to scan large DNA sequences with thousands of annotated features. The map can be in a circular or linear format. Customize the display of enzyme sites, features, primers, ORFs, DNA colors, and more. SnapGene is the easiest way to plan, visualize, and document your everyday molecular biology procedures.
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