Snapgene viewer change color simulator#
Snapgene viewer change color windows#

Snapgene viewer change color windows#

Fixed an issue where the bases in sequence view could jump around when using a Windows computers with multiple screens.

(Reported by Leslie Bembinster and Mily Ron) Fixed an issue where empty lines with tabs or spaces resulted in an erronous message being displayed when importing primers from a list.Substituted estimated quality data for nonsensical embedded quality data that is present in some otherwise valid sequence trace files, and enabled alignment of those sequence traces.Enabled SnapGene to tolerate and ignore dashes when opening FASTA files.Prevented an occasional issue in which spin boxes would be gray rather than showing the current value.Fixed issues with printing agarose gels on Windows.Removed an outdated note about DTT from the enzyme description for BsmBI.(Reported by Wulf Dirk and Megha Rajendran) Improved the alignment algorithm to reduce the likelihood of displaying an unwanted alignment with a large gap.Improved the MacVector importer to decode all features as features rather than colored ranges, and to decode qualifiers and feature names more reliably.

Ensured that qualifiers are displayed properly when printing Features and Primers views.

Snapgene viewer change color simulator#

Enhanced the Gateway simulator to record custom names of Entry clones in the history.Prevented an occasional issue in which multiple copies of a feature were annotated when detecting common features.Ensured that the “Circularize” command will work after amplifying a fragment that began at the numerical origin.Improved the display of aligned sequences that have long names containing carriage returns.Implemented numerous optimizations and textual enhancements.Added a “User Guide” link to the Help menu.Enhanced the topology indicator to bring up the Circularize or Linearize dialog.Added recognition for Spacebar as a command to page down in all views.Enabled the simultaneous editing of the display priority for multiple features at a time.Enabled copying of the translation of two or more consecutive segments in a feature, even if the segments are separated by an intron.Improved the detection of common features by their protein translation in situations where the first or last amino acid may not be present in a relevant match.Improved the default phosphorylation of newly created sequences.Turned off the default prioritization for display of newly created features.Improved sequence trace quality estimation.Improved topology detection when using the New DNA File dialog.Improved the detection of regulatory features.Added tooltips to the type and qualifier controls in the feature dialogs.Improved the default name used by the New File from Selection dialog in many contexts.Enhanced export of primer data to include options for primer length, % GC, and MW.Enabled export of all primer data if no primers are selected.Enabled drag and drop for opening files in the launch dialog, or loading files in an action dialog, or aligning sequences with the alignment list box.Modified the Import Primer from a List dialog to choose by default the last list used.Modified the Add|Import|Detect Features|Primers dialogs to remember the last column used for sorting.Added the ability to detect common features in inserted sequences.Configured the default behavior to open documents and windows on the primary display, or if other windows have been opened, on the last display that was used.Improved zooming into selected features and primers when no DNA selection is present.New “Symbols and Abbreviations” window, accessible from the Help menu.New “Analyze Selected Primer(s)” command in the Primers menu, for direction to IDT’s OligoAnalyzer website.Support for the following GenBank feature qualifiers:.Support for the following GenBank feature types:.Opening of previously generated alignments in SnapGene Viewer.Highlighting of matches for searches in both the view and the relevant scroll bar.Japanese language option for the entire interface.SnapGene can now open the following protein file formats: DNADynamo, DNASTAR (EditSeq, SeqBuilder) DNA Strider FASTA, GenBank/GenPept MacVector Vector NTI (pa4, pro, and VNTI database) Support for standalone protein sequence files, including conversion from translated DNA features to protein sequences.Changes in version 3.0 (Dec 21, 2015) New Functionality