Date: 9/29/2016 Version Affected: Version 13 and previous Version Fixed: 14.0 Issue: By December 31, 2016, all U.S. federal government entities will be required to use secure “https” websites instead of general “http” websites. The National Center for Biotechnology Information (NCBI) has announced they plan to make this change on September 30, […]
Date: 9/29/2016 Version Affected: 13 and previous Version Fixed: 14.0 Issue: The National Center for Biotechnology Information (NCBI) has announced that they are changing certain file formats and restructuring their EUtils databases. The date of this change has not been announced, but will likely occur in Fall 2016. Many Lasergene applications […]
MADISON, Wisconsin – September 30, 2016 – DNASTAR® announced the release of Lasergene 14 today, which includes a broad range of improvements in DNA, RNA and protein sequence and structure prediction and analysis. Lasergene 14 includes three brand new applications: GenVision Pro, a comprehensive genome browser; NovaDock, a protein-protein docking application; and NovaFold Antibody, a […]
Join us for our first Lasergene 14 webinar next week when DNASTAR Vice President and General Manager, Tom Schwei, will present a 30-minute overview of Lasergene 14. Lasergene 14: New Software for a Changing Biological Landscape Wednesday, October 5th at 12:00 pm EDT
Did you know that Lasergene Genomics Suite now includes access to the Variant Annotation Database (VAD) for human sequencing data? Check out our recent interview with Dr. Tim Durfee, who explained how the tool works and how it can help genomics and clinical researchers with their variant analysis.
We know that not everyone needs a comprehensive molecular biology software package — sometimes you just need the basics. Now the most trusted name in sequence analysis software is offering those essentials everyone needs, and at a price that most everyone can afford —just $650 for the first license (academic and government researchers).
Lasergene Genomics Suite now includes access to the Variant Annotation Database (VAD) for human sequencing data. I recently spoke with DNASTAR Scientist, Dr. Tim Durfee about the VAD to get a better understanding of how the tool works and how it can help genomics and clinical researchers with their variant analysis. Can you describe what […]
We are excited to announce the upcoming release of Lasergene 14, which will be available to download in the next several weeks. Check out our preview video to get a sneak peek at all the features in Lasergene 14, from enhanced cloning to genome visualization to protein docking, and much more!
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