A complex field such as molecular biology requires efficient ways to visualize gene sequences and associated data. SnapGene Viewer for Mac helps you better visualize, annotate, and simulate DNA-related procedures.
Installing SnapGene Viewer for Mac is quick and easy. At first launch a setup screen pops up that lets you define your preferred enzyme suppliers. You are also invited to watch an introductory video to guide you through the basic functions of the software. Six more videos are also available to explore advanced functions of this program. Many screenshots and feature descriptions that will help you learn more about the program and whether it's able to fulfill your needs are available at the developer's Web site. No manual seemed readily available. The viewer is free so you can communicate your work with colleagues with no need for additional licenses on their end. The program felt well engineered and stable. Unfortunately, the demo version won't let you test the actual simulations of molecular biology procedures. On the plus side, annotations and viewing and searching functions are available on the demo and viewer versions. A sample file is provided to let you quickly dig into the core functionality of the software and determine if it is right for you.
SnapGene Viewer for Mac seems suited for biology labs or researchers who are looking for an efficient and ergonomic gene visualization solution that provides annotations and simulation of molecular biology procedures.
SnapGene Viewer is revolutionary software that allows molecular biologists to create, browse, and share richly annotated DNA sequence files up to 1 Gb in length. It is a great tool for both research and teaching. Here are some of the things you can do with this software. Create a DNA sequence file by either entering a sequence, or importing a record from GenBank, or opening an annotated sequence stored in one of many common file formats. Browse or print a DNA sequence and its annotations using customizable Map, Sequence, Enzymes, Features, Primers, and History views. Search a DNA sequence to match either a DNA query, or a protein translation, or an annotation. Open and edit sequence trace files. Automatically annotate common features, or manually annotate coding sequences and other features. Design and annotate primers for PCR, sequencing, or mutagenesis. Identify open reading frames (ORFs) with a single mouse click. Export a plasmid map as an image, or export an annotated DNA sequence to GenBank format. Freely share data with your colleagues or customers using the universally accessible SnapGene format.