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What’s New in SnapGene 5.0.7 Crack
New tools added for its user.
More simple and faster.
Hence, better than the old version.
Added tools for pairwise alignment of DNA and protein sequences. (Requested by many customers)
Added interfaces for simulating directional and blunt TOPO® cloning. (Requested by many customers)
Provided support for customizing the background window color.
Added the ability to drag out and view non-aligned ends of aligned sequences. (Requested by just about everyone)
Added the ability to display feature translations in lowercase. (Requested by Peter Drain)
Enabled alignments to be constrained to a designated strand or region of the reference DNA sequence. (Requested by Christel Aebischer and others)
Added the ability to import sequences directly from Ensembl. (Requested by Jaeho Ryu, Elena Fujiwara, and others)
Enabled the calculation and saving of codon frequencies for one or more translated features. (Requested by Craig VanDolleweerd and Jeanie Lin)
Enabled feature visibility to be toggled by feature type. (Requested by Di Xia and Lee-Chung Lin)
Added the option to trim low-quality ends when importing sequence traces for contig assembly or multiple sequence alignment.
Enabled an aligned cDNA to be used to annotate a feature with exons and introns. (Requested by Rob Steele and Peishan Yi)
Added support for opening DNASIS files. (Requested emotionally by Jim Galen)
Enhanced BLAST support to provide all five options (blastn, blastx, tblastx, blastp, and tblastn). (Requested by Inbar Plaschkes)
Updated the “Aligned Sequences” menu when viewing an alignment to a reference sequence, and added the following new commands: • Duplicate Selected Sequence(s) in New Window(s) • Remove All Sequences • Show/Hide Quality Data for Sequence Traces
Added a control in Preferences to enable quality data for sequence traces to be shown by default when aligning to a reference DNA sequence.
Enabled a selected portion of a multiple DNA alignment to be converted to a multiple protein alignment. (Requested by Walid Azar)
Added a control for exporting selected files in a collection as a list in PDF or tab-separated format. (Requested by David Murray)
Added a “Choose DNA Sequences…” button to the Simulate Agarose Gel dialog, as a shortcut for configuring multiple lanes. (Requested by Dhaval Bhatt)
Enabled amino acid sequences to be copied as either 1- or 3-letter amino acid codes. (Requested by Moo-Hyung Lee)
Enabled the copying of selections that span multiple lines in pairwise or multiple alignment windows.
Added the New England Biolabs “TriDye™ Ultra Low Range DNA Ladder”.
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