Corrected an issue with saving aligned reads to an ssDNA sequence.Fixed an issue that sometimes prevented showing the first aligned sequence when printing an alignment to a reference sequence.(Requested by Jadyn Cox, Hsinho Huang, and Sara Smith).Increased the number of primer binding sites that can be shown in Map view.Fixed a regression that prevented the display of some primer binding sites when simplified hybridizations are being shown.Ensured correct reporting of the number of matches when searching ssDNA sequences.Addressed a stability issue with viewing some primers in Sequence view.Addressed an issue with folders in collections stored on network drives.(Reported by Christine Chidester, Lauren Flynn, and Clifford Dustin Rubinstein).Corrected an issue with showing aligned sequences as double-stranded DNA.Pricing varies with usage, license type, and the number of seats, as can be seen here. Thanks to SnapGene Viewer, the files can be shared with colleagues around the world. The streamlined interface supports a range of cloning and PCR manipulations. SnapGene offers the fastest and easiest way to plan, visualize, and document your molecular biology procedures.
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