Date: 9/30/2021 Version Affected: Lasergene 17.3.0.58 and earlier Version Fixed: Lasergene 17.3.0.59 and later Issue…
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Did you know that DNASTAR has been pioneering software solutions for life scientists since the...
Learn more about PacBio HiFi sequencing, a hybrid of short- and long-read sequencing that is extremely accurate and is especially useful for de novo genome assembly.
Watch our 1-hour webinar on how to master viral genome analysis.
DNASTAR announced today the release of Lasergene 17.3, which includes new features and functionality focused on genomic analysis and variant identification supporting COVID-19 research.
Focused on COVID-19 research, Lasergene 17.3 includes a new workflow for long read viral genome assemblies, a new MAFFT7 alignment algorithm to quickly align thousands of viral genomes, and much more.
Watch our 1-hour webinar on how to create the most accurate assemblies of your Sanger sequencing data.
DNASTAR software is trusted by over 80,000 researchers in academia, government, and industry. Learn why so many people turn to DNASTAR for their sequence and structure analysis needs.
DNASTAR is utilized by thousands of researchers around the world, including scientists at over 500 biotech and pharmaceutical companies, including every pharmaceutical company on the Fortune 500 list. Why do so many scientists in industry trust DNASTAR? Read on to find out!
DNASTAR software is trusted by over 1200 colleges and universities around the world. Learn how DNASTAR customers are using Lasergene in an academic setting.
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