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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...

Using Lasergene to De Novo Assemble PacBio HiFi Data

Learn more about PacBio HiFi sequencing, a hybrid of short- and long-read sequencing that...

Answers to your “Genomic Data Assembly Strategies” webinar questions

Check out our new post featuring questions and answers from our recent webinar on...

How to Assemble Genomes like a Bioinformatics Pro

Whether you are working with Illumina, Oxford Nanopore, PacBio data, or a combination of...

Genome Polishing Benchmarks: SeqMan NGen vs. Three Open-Source Tools

See how SeqMan NGen stands up to three open-source tools using data from PacBio...

Steps for annotating and analyzing multi-sample variant data in Lasergene. DNASTAR software tools and supplemental data are shown in orange.

Working with Variant Call Format Files in Lasergene Genomics

DNASTAR's Variant Annotation workflow provides functional annotation and enriched information for analyzing human samples...

Is Open Source NGS Software for You?

An interview with Eric Cabot Ph.D. Dr. Eric Cabot received his MS from the...

Q&A: NGS Sequence Assembly on the Cloud

Get your 5 FREE Cloud Assemblies! What is “Cloud Assemblies”? It’s a new service...

Free NGS Assembly and Alignment for Genomic Sequencing Data

We know that for many researchers, performing large scale next-generation sequence alignments or de...

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