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, … Continue reading →

    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 … Continue reading →

    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 … Continue reading →

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 … Continue reading →

    Check out our newest video to see three different ways to find and compare genes and variants of interest for a variety of genomics and transcriptomics projects, including whole genome and exome assemblies, RNA-Seq and ChIP-Seq alignments, and … Continue reading →

Whether you are working with NGS or Sanger data, whole genome sequencing or targeted resequencing, Lasergene provides highly accurate assembly and variant detection for every project. Check out these 10 recent publications citing Lasergene for variant analysis for genome and exome projects, … Continue reading →

  In the latest installment of DNASTAR LabViews, we speak with Dr. Richard Buick of Fusion Antibodies to find out how his group uses NovaFold software as part of their antibody humanization service. Check out the interview below to learn more … Continue reading →

  This week, we’re sharing a video featuring one of our most popular workflows: Sanger sequence assembly and analysis in Lasergene Molecular Biology Suite. See how easy it is to assemble read data ­de novo or against a reference sequence, … Continue reading →