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Latest Version
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Operating System
Windows 7 / Windows 7 64 / Windows 8 / Windows 8 64 / Windows 10 / Windows 10 64
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User Rating
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Author / Product
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Filename
snapgene_5.2.4_win.exe
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MD5 Checksum
c1e446f840136c689e06b9a8b9cb0f02
Sometimes latest versions of the software can cause issues when installed on older devices or devices running an older version of the operating system.
Software makers usually fix these issues but it can take them some time. What you can do in the meantime is to download and install an older version of SnapGene 5.2.4.
For those interested in downloading the most recent release of SnapGene or reading our review, simply click here.
All old versions distributed on our website are completely virus-free and available for download at no cost.
We would love to hear from you
If you have any questions or ideas that you want to share with us - head over to our Contact page and let us know. We value your feedback!
What's new in this version:
New Functionality:
- Added DNA ladders from GeneBio Systems
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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