If you’re a frequent visitor to our website or this blog, you’ll know we talk a lot about accuracy here. When it comes to your research, we understand that obtaining accurate and reliable results is paramount in deciding which … Continue reading
We’ve run the numbers and we are proud to announce that DNASTAR software continues to be the most widely cited sequence analysis software in peer-reviewed journals. To date, our software has been cited over 65,000 times. In 2016 alone, … Continue reading
The DNASTAR YouTube channel features hundreds of videos covering workflows for molecular biology, next-gen sequence analysis, and protein structure prediction. Whether you want to do virtual cloning on a desktop computer or multiple genome assemblies on the cloud, large scale … Continue reading
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 … 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
I recently spoke with Dr. Richard Buick, Chief Technical Officer 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 about antibody humanization, and … Continue reading
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