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Lasergene 17.4.2 Release Notes

Lasergene 17.4.2 is a minor release that includes improvements to the Variant Table in MegAlign Pro and a bug fix addressing an issue with merging unaligned sequences.

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...

Sequence Analysis

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...

Genomics

Using Lasergene to De Novo Assemble PacBio HiFi Data

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

Sequence Analysis

Answers to your “Phylogenetic Tree” webinar questions

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

Sequence Analysis

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...

Transcriptomics

De novo Transcriptome Assembly: SeqMan NGen vs. CLC Genomics Workbench

Do you need to assemble RNA-Seq de novo transcriptome data as part of your...

Sequence Analysis

Two ways to find the best MegAlign Pro multiple sequence alignment method for your data

If you’re doing a whole-genome alignment in MegAlign Pro, Mauve is the best MegAlign...

Transcriptomics

RNA-Seq Assembly and Normalization Methods—an Interview with Dr. Carl-Erik Tornqvist

RNA-Seq transcriptome projects can be complex. In this post, DNASTAR’s Manager of Sales and...

Genomics

Answers to your “Genomic Data Assembly Strategies” webinar questions

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

An Integrated Solution for De Novo Transcriptome Analysis

DNASTAR BLOG

Lasergene 17.4.2 Release Notes

Variant Annotation with Lasergene Genomics: The easy way to discover, annotate and filter sequence variants

Using the MAFFT alignment algorithm for high-capacity viral genome alignment

Using Lasergene to De Novo Assemble PacBio HiFi Data

Answers to your “Phylogenetic Tree” webinar questions

How to Create the Best Phylogenetic Tree for Your Data Using MegAlign Pro

De novo Transcriptome Assembly: SeqMan NGen vs. CLC Genomics Workbench

Two ways to find the best MegAlign Pro multiple sequence alignment method for your data

RNA-Seq Assembly and Normalization Methods—an Interview with Dr. Carl-Erik Tornqvist

Answers to your “Genomic Data Assembly Strategies” webinar questions