SnapGene Version 6.0.3
SnapGene 6.0.3 was released on April 17, 2022.
Enhancements
- Improved formatting when using the Copy Selected Primers and Export Primer Data commands.
(Requested by Di Xia) - Improved responsiveness of cloning dialogs when switching tabs and flipping fragments.
- Improved responsiveness when making selections in multiple sequence alignments.
- Improved responsiveness when performing or opening a file with an alignment to a reference sequence.
Fixes
- Fixed an issue with renaming folders in collections.
(Reported by Dinesh Babu Paudel) - Avoid switching from Map to Sequence view after importing sequences to align to the reference.
(Reported by Cary Valley and Michal Poborsky) - Fixed an regression where features in replaced regions were erronously retained during restriction cloning if the insert was the same size.
(Reported by Martha and James Smart) - Fixed an issue with decoding features from GenBank files generated by CHOPCHOP.
(Reported by Reuben Philip) - Fixed aligning sequences in a multi-sequence FASTA file with a reference.
(Reported by Fang Suo, Louise La Barbera Kastberg, Guttorm Haraldsen, and Ryan McNulty ) - Fixed an issue with opening supported file types in Miscellaneous Files when viewing a collection.
(Reported by Dinesh Babu Paudel) - Fixed a default file name and extension when saving a sequence trace.
(Reported by Dinesh Babu Paude) - Addressed an issue where Sharepoint index conflict files resulted in new file notifications when working with collections.
(Reported by Andras Solt) - Improved stability when detecting common features.
- Fixed an issue where the selection bar was blank after making a feature in a multiple sequence alignment.
- Fixed a crash when attempting to create a custom feature type in SnapGene Viewer.
- Fixed an issue that prevented loading non-installed custom feature types that are embedded within a file.
- Improved stability with multiple sequence alignments.
- Fixed a memory leak when creating, editing, or duplicating features.
- Corrected an issue with history colors after performing PCR using primers that extend beyond the end of a linear template.
- Fixed an issue with making RNA sequences from selections in large genomic sequences.
- Fixed an issue where unnecessary menus were sometimes shown on the launch dialog.
- Fixed various issues where characters right of a period in a agarose gel sequence name was not shown in the fragment list or source control
- Removed unecessary message indicating upgrading to SnapGene is required to perform an alignemnt if one or more aligned sequences and an associated alignment to the reference sequence is already computed.
- Improved overall stability
- Addressed various memory leaks.
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