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Snapgene viewer quality2/12/2024 MASS PCEP will be administered and coordinated by MASS. To create a map image the input must be a DNA sequence in a SnapGene. SnapGene Viewer is free software that allows molecular biologists to create. Please make your choice based on your computer platform and operating system. Ensure the SnapGene Application/Program is not running before you attempt to run the executable from the command line. You will find information about downloading, installing and using the software. Click on the appropriate icon(s) to go to the respective Web page. Tools for Viewing Sanger Sequencing Data Sequence / Chromatogram Viewing SoftwareĪ number of free software programs are available for viewing trace or chromatogram files. Azenta Life Sciences Consumables & Instruments.Gene Synthesis & Cloning/Mutagenesis FAQs.CLIA Variant Confirmation (PCR + Sanger).SnapGene offers the fastest and easiest way to plan, visualize, and document your molecular biology procedures. The streamlined interface supports a range of cloning and PCR manipulations. Thanks to SnapGene Viewer, the files can be shared with colleagues around the world. Pricing varies with usage, license type, and the number of seats, as can be seen here. Corrected an issue with showing aligned sequences as double-stranded DNA.(Reported by Christine Chidester, Lauren Flynn, and Clifford Dustin Rubinstein). ![]() ![]() Addressed an issue with folders in collections stored on network drives.Addressed a stability issue with viewing some primers in Sequence view.Ensured correct reporting of the number of matches when searching ssDNA sequences.Fixed a regression that prevented the display of some primer binding sites when simplified hybridizations are being shown.Increased the number of primer binding sites that can be shown in Map view.(Requested by Jadyn Cox, Hsinho Huang, and Sara Smith).Fixed an issue that sometimes prevented showing the first aligned sequence when printing an alignment to a reference sequence.Corrected an issue with saving aligned reads to an ssDNA sequence.Improved stability when expanding sequences aligned to a reference DNA sequence.Improved stability when choosing alternative codons.Ensured that opened documents are always added to the recent files list.Fixed an issue that could prevent enzymes from being displayed in older documents in collections.Ensured that display options are always preserved when duplicating collection documents in a new window.Removed a blank cascading menu that could appear in the Edit menu when using “Save As”.Improved stability when dragging trimming handles.Improved stability when using Opt-click to invoke “Close All Open Files” on macOS.Improved the appearance of the focus ring for comboboxes on macOS.Improved the mnemonic shortcut for deleting a restriction fragment on Windows.Improved the default filename when exporting an alignment.Prevented unnecessary scrolling when undoing sequence modifications. ![]()
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