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?
Watch our 1-hour webinar to learn how to easily analyze transcriptome data for non-model organisms.
Watch our 1-hour webinar designed to help new users understand the available functionality in Lasergene and how to get started with the work they want to do.
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.
Do you need to assemble RNA-Seq de novo transcriptome data as part of your research?
Watch our 1-hour webinar on best practices for aligning and analyzing RNA-Seq data using the…
RNA-Seq transcriptome projects can be complex. In this post, DNASTAR’s Manager of Sales and Client…
Check out our new post featuring questions and answers from our recent webinar on genomic…
Whether you are working with Illumina, Oxford Nanopore, PacBio data, or a combination of these…
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