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SnapGene Viewer is revolutionary software that allows molecular biologists to create, browse, and share richly annotated DNA sequence files up to 1 Gbp in length. What are the differences between SnapGene and the free SnapGene Viewer? See what you’re thinking.

Version 5.2.4:

New functionality:

• Added DNA ladders from GeneBio Systems.

• Create a New Account.
• How can I obtain a protein sequence from a SnapGene file? Printing and Exporting. How do I export my Map or Sequence as a vector-based graphic? Why do I see missing or garbled text after printing to a PDF file? Sequence Traces. What base caller does SnapGene use for sequence traces? Citing SnapGene. How should I cite SnapGene or SnapGene Viewer?
• SnapGene Viewer is software that allows molecular biologists to create, browse, and share richly annotated DNA sequence files up to 1 GB in length. Features include visualize: Create a DNA sequence.
• 8/10 - SnapGene Viewerを無料ダウンロード SnapGene Viewerを利用すればDNA配列データ、すべてのデータを確認するための適切なソフトウェアを利用出来ます。.

Fixes:

• Improved application stability when dragging out selections.
• Corrected a regression to ensure detection of restriction sites whose recognition sequences span the numerical origin.
• Populate the 'Description' fields when pasting GenBank content into the New File dialogs.
• Improved the detection of sequence type when importing DNASTAR SeqBuilder files.
• Corrected a regression to restore transfer of primers when pasting a copied DNA sequence.
• Fixed an issue that could result in editing-induced disappearance of a sequence aligned to a reference DNA sequence.
• Enabled simulation of Gateway BP and LR recombination around the numerical origin.
• Improved application stability when searching for enzymes, features, and primers.
• Corrected a misleading message that was shown when a problem occurred during program activation.
• Ensured that the enzyme set indicator does not occlude content after scrolling to the bottom of Sequence view.
• Streamlined the side toolbar in the Insert Codons, Choose Alternative Codons, Browse Common Features and Insert Feature dialogs.
• Restored highlighting of the called base under the mouse when viewing sequence traces.
• Improved application stability when using the 'Find similar DNA sequences' command.
• Improved performance when showing the Add Primer dialog and other dialogs that provide controls for choosing files.
• Ensured highlighting of the inserted region for Gateway BP cloning in the Insert tab, and of the ancestral insert in History view for the resulting product file.
• Restored import of ssRNA sequences as double-stranded rather than single-stranded DNA.
• Prevented repetitive alignment to a reference sequence when making simple edits such as insertions, deletions, and same-size replacements.
• Ensured that the Next button is the default control after searching a sequence trace.
• Ensured correct scrolling of Sequence, Features, and Primers views in response to a change in the selection, but only when appropriate.
• Improved application stability when quitting.
• Improved application stability when hovering over aligned sequences.
• Improved application stability when mousing over features.
• Improved application tability when searching a collection for a named feature.
• Improved application stability when importing primers.
• Improved reliability when importing from NCBI.

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A user-friendly software solution that can come in handy for previewing your created DNA maps

SnapGene Viewer is an excellent tool for viewing DNA maps with ease. It works very well in conjunction with Snapgene, a software that lets you create and edit DNA sequences and maps. The viewer allows anyone to see created DNA maps and works with big files, with a limit of 1Gb per file.
An excellent feature of SnapGene Viewer is the ability to export a DNA sequence from the given map and save it as a GenBank format for further use and analysis. While the application itself has just a couple of features compared to its main SnapGene application, it's useful however for collaboration purposes or just to view different sequences quickly and with ease.
Overall, SnapGene Viewer just as SnapGene, it's aimed more towards academic research and while the tools come with complex terminology and features, the viewer is a bit more accessible for viewing different DNA maps or sequences.

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