Best practices for molecular biology, genomics, protein and bioinformatics research.
Once you find thousands of variants in a set of samples, how can you easily do variant annotation and identify which ones are of the greatest importance?
We recently sat down with Matt Keyser, DNASTAR Senior Product Manager, to ask what makes the MAFFT v.7 multiple sequence alignment (MSA) algorithm special and how to use it within MegAlign Pro.
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.
Protein sequences are published at an exponentially higher rate than protein structures. Elucidating a protein…
If you’re doing a whole-genome alignment in MegAlign Pro, Mauve is the best MegAlign Pro…
RNA-Seq transcriptome projects can be complex. In this post, DNASTAR’s Manager of Sales and Client…
Whether you are working with Illumina, Oxford Nanopore, PacBio data, or a combination of these…
Check out our new “Frequently Asked Questions” post based on customer questions at our recent…
Check out our new “Frequently Asked Questions” post based on customer questions at our recent…
Written by Eric Cabot, PhD With the latest version of Lasergene, MegAlign Pro, part of...
© 2022 — DNASTAR Privacy Policy
Most Commented Posts