DNASTAR’s Structural Biology Suite includes epitope prediction methods that allow you to predict B-cell epitopes based on protein sequence data. You can then view predicted epitopes and antigenic regions along your sequence and structure and compare predictions to other … Continue reading →

  This week, get insider tips and tricks on de novo genome assembly from Senior Manager of NGS Applications Matthew Keyser. Our most recent blog post details how to assess your RAM needs based on your data type and desired coverage. … Continue reading →

  DNASTAR’s MegAlign Pro application allows you to generate phylogenetic trees to predict evolutionary relationships. You then have the ability to customize these trees in terms of color, layout, and styling options for use in your publications. Finally, you also … Continue reading →

  With decreasing costs of obtaining next-generation sequencing data, the challenge becomes less about available data and more about researchers determining meaningful correlations. The right data analysis tools facilitate discovery of the solutions to Mendelian and complex diseases, and DNASTAR … Continue reading →

  Will you be at the European Society of Human Genetics meeting in Glasgow? Join DNASTAR’s Jackie Carville at booth #740 anytime between June 6th and June 8th.  Learn more about our software supporting human genome, exome, and gene panel assembly, … Continue reading →

Will you be at the American Society for Microbiology meeting in New Orleans? Join DNASTAR’s Jackie Carville and Brian Anderson at booth #711 anytime between May 31st and June 2nd.  Learn more about our software supporting microbial genome assembly and analysis, … Continue reading →

Are you searching to find the perfect next-gen sequence assembly and analysis software for your project? This week, we present five considerations when it comes to selecting a software package that fits all of your needs. Read our blog post … Continue reading →

We invite you to register for our upcoming webinar.   In this free webinar, to be held on Wednesday, May 20th at 11:00 am EDT, DNASTAR’s Matt Keyser will discuss our support for assembly and analysis of next-gen microbial data. Explore how … Continue reading →

  Please join us at the BioConference Live Genetics and Genomics event from May 13th to 14th. DNASTAR’s Matthew Keyser will be presenting a talk entitled “DNASTAR Software For Accurate Variant Detection and Validation in Targeted Gene Panel Data Sets” … Continue reading →

  DNASTAR’s automated genome closure workflow allows you to save valuable time and resources by greatly reducing the need for manual finishing of your assembled project to address gaps caused by structural variants, such as insertions and deletions. De novogenome closure … Continue reading →