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Lasergene 18 Release Notes
The Lasergene 18 release brings significant new features and improved functionality, including a major update to GenVision Pro, our application for visualizing and analyzing genomic data.
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What Can We Learn from Gene Homology Analysis?
This blog post answers some common questions about sequence homology and how to use...
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Q&A: Assembling and Analyzing NGS & Long Read Sequences
This post answers some recent DNASTAR customer questions related to NGS and long read...
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Free NGS Assembly and Alignment in the Cloud
Whether you've licensed Lasergene or want to do a free trial, you automatically get...
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Variant Annotation with Lasergene Genomics: The easy way to discover, annotate and filter sequence variants
Once you find thousands of variants in a set of samples, how can you...
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Using the MAFFT alignment algorithm for high-capacity viral genome alignment
We recently sat down with Matt Keyser, DNASTAR Senior Product Manager, to ask what...
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DNASTAR: Enabling Life Science Discovery Since 1984
Did you know that DNASTAR has been pioneering software solutions for life scientists since...
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Using Lasergene to De Novo Assemble PacBio HiFi Data
Learn more about PacBio HiFi sequencing, a hybrid of short- and long-read sequencing that...
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Answers to your “Phylogenetic Tree” webinar questions
Check out our new post featuring questions and answers from our recent webinar on...
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How to Create the Best Phylogenetic Tree for Your Data Using MegAlign Pro
Protein sequences are published at an exponentially higher rate than protein structures. Elucidating a...
An Integrated Solution for De Novo Transcriptome Analysis
