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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_viewer_5.1.4_win.exe
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MD5 Checksum
68e04d331a9a2e258e499f90d6165793
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 Viewer 5.1.4.
For those interested in downloading the most recent release of SnapGene Viewer 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 support for importing protein features from the GFF3 format
- Enabled features to be preserved when a replacement leaves the sequence length unchanged
Enhancements:
- Enabled the import of custom user fields from Vector NTI databases
- Increased the 3' match length limit to 25 bases when importing primers from a list
- Enabled capture of the history of a protein translated from DNA when importing from Vector NTI Advance
- Enhanced primer tooltips to include % GC for the annealed region
- Improved copy and paste of sequence alignments into text editors and other programs
- Increased the size of the DOI field when editing references
- Made various color, layout, and textual enhancements
Fixes:
- Mandated use of the proper default font size when creating new files, importing from online, and opening non-native files
- Corrected an issue that prevented importing primers into multiple files in a collection
- Corrected a regression with displaying translations and the "Original Sequence" when no sequences are aligned to the reference DNA sequence
- Enabled changing methylation for placeholder files
- Fixed various issues when working with placeholder files
- Implemented automatic correction of invalid alignments to a reference sequence computed with prior versions
- Fixed an issue that prevented manually specifying the zoomed range
- Corrected the "+" symbol in plasmid names when importing from "SnapGene Online Sequences"
- Ensured correct updating of the zoomed range when navigating to matches with the Find tool
- Addressed an issue with specifying the position of protein interchain bond locations
- Removed the "Codons" cascading menu when interacting with protein sequences
- Corrected an issue that prevented importing multi-sequence GenBank and GenPept files into a collection
- Ensured that translation numbering is maintained when using Make Protein from multiple selected translated features
- Ensured that the match threshold controls are listed only once when importing features from a SnapGene file
- Corrected an issue that could cause file names to be clipped in source menus
- Fixed an issue that caused files to be marked as modified after hovering over hyperlinks in the Description Panel
- Ensured that stop codons present in protein query strings are included in the search results
- Improved the import of multi-part qualifiers from Geneious
- Fixed an issue with undo of sequence color changes that are limited to a single strand
- Corrected the "Copy" shortcut when viewing a protein sequence or multi-protein alignment
- Ensured more robust behavior when adding primers to DNA sequences
- Turned on the display of truncated primer description data when full descriptions are toggled off in Primers view
- Corrected an issue in which simplified primer binding sites were not shown after modifying hybridization parameters
- Ensured that sufficient space is always allocated above displays of complex primer binding sites in Sequence view
- Turned on display of the parental enzyme set when viewing Nicking Endonucleases in Sequence and Map views
- Improved reliability when importing from Addgene
- Improved the import of Addgene sequences that contain slashes in their names
- Ensured that side toolbar buttons in dialogs are not hidden
- Corrected a regression in which two copies of common features such as EGFP were sometimes annotated when detecting common features
- Removed "Match Threshold" controls from the "Add to Common Features" dialog
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