SnapGene Viewer6.0.1

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About SnapGene Viewer

SnapGene Viewer is a powerful and user-friendly software tool designed for molecular biologists and researchers to visualize and analyze DNA sequences.

SnapGene Viewer provides an intuitive interface that allows users to easily load, view, and analyze DNA sequences in various formats, including GenBank, FASTA, and SnapGene files. Users can navigate through sequences, zoom in and out, and scroll through large DNA molecules with ease. The software also offers a rich set of tools for visualizing DNA features such as genes, promoters, restriction sites, and annotations, making it easy to analyze and annotate DNA sequences.

One of the key features of SnapGene Viewer is its ability to simulate DNA cloning and PCR reactions. Users can design and simulate DNA cloning experiments by selecting and dragging DNA fragments, enzymes, and vectors onto a virtual DNA map. The software automatically checks for compatibility and displays the results in a graphical format, helping users plan and optimize their molecular cloning experiments.

In addition to visualizing and simulating DNA cloning, SnapGene Viewer also provides tools for designing and editing DNA sequences. Users can create new DNA sequences, edit existing sequences, and annotate them with features such as genes, markers, and primers. The software also includes a comprehensive set of tools for primer design, including automatic primer suggestions based on the selected DNA sequence.

Overall, SnapGene Viewer is a versatile and user-friendly tool that provides molecular biologists and researchers with a powerful platform for visualizing, analyzing, and designing DNA sequences. Its intuitive interface, robust features, and simulation capabilities make it an invaluable tool for molecular biology research and DNA manipulation.


Key Features:

  • DNA sequence analysis and visualization.
  • Plasmid map design with drag-and-drop features.
  • Primer design for PCR amplification.
  • DNA simulation for virtual cloning experiments.
  • File management for organizing and sharing DNA sequences.
  • Collaborative features for sharing and collaboration.
  • Customizable annotation styles for DNA sequences.


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