DNASTAR Lasergene 15 Suite Full Download + crack
Whether your work focuses on next-gen sequencing assembly and analysis, clinical research, or traditional sequence analysis, the DNASTAR Lasergene package will meet your research needs, and is available on both the desktop computer as well as the DNASTAR Cloud.
What's new in Lasergene 15?
We are pleased to announce the release of Lasergene 15, a major upgrade to the DNASTAR Lasergene Suite. This release is very exciting for us, in part because it includes a complete overhaul of SeqBuilder, the foundation of our Molecular Biology Suite. In fact, the revamp was major enough that we felt it needed a new name — SeqBuilder Pro. Enjoy all of the functionality you know and love, but with a more intuitive and streamlined design.
This release also includes significant enhancements to our Structural Biology and Genomics suites.
For our Lasergene Molecular Biology Suite customers, this is huge. SeqBuilder has morphed into a much more intuitive and streamlined application we're calling SeqBuilder Pro. Don't worry, all of the functionality you know and love is still there: sequence map creation, primer design, virtual cloning, and all the rest, but it's easier and more intuitive to use! The most obvious change is a new state-of-the-art look and feel that is consistent with many other Lasergene applications. Now you can easily navigate between synchronized views with a click of a button, and rearrange views and toolbars by simply dragging and dropping them where you want them to be.
We've also improved upon many of the functions you rely on, such as creating sequence maps. New zoom-level sliders and an auto-placement for large groups of restriction enzymes makes creating the perfect map a breeze. You can also now quickly search and select enyzmes with our new responsive search feature. For our long-time users who still use our legacy EditSeq application, we've added a new "compact view" that mimics the EditSeq layout. Views that list items like features and primers can now be collapsed, expanded, and sorted to easily find and edit what you're looking for. Speaking of features, SeqBuilder Pro supports multiple selection, so if for example, you want to find all the features of a certain type and change the style, it's just a couple of clicks away.
If you are familiar with Lasergene Genomics Suite, you'll know that for years, we've ranked #1 in accuracy for NGS alignments and variant calling. In Lasergene 15, we're offering an option to further fine-tune our accurate variant detection method by adding a new enhanced read mapping option for whole genome alignments. This option gives users a choice to either use the default variant detection parameters, which offers the fastest alignment, or dramatically reduce the detection of false positives identified during SNP calling, by using the new option. Your objective for each project may be different, so the choice is yours.
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