Do you need to assemble RNA-Seq de novo transcriptome data as part of your research? If so, you might want to consider DNASTAR’s SeqMan NGen, part of the Lasergene Genomics package. SeqMan NGen provides an integrated solution that’s easy to use: from setup to downstream analysis.
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…
Watch our 1-hour webinar for an in-depth look at different assembly strategies for genomic sequencing…
See how SeqMan NGen stands up to three open-source tools using data from PacBio…
DNASTAR’s Variant Annotation workflow provides functional annotation and enriched information for analyzing human samples in…
An interview with Eric Cabot Ph.D. Dr. Eric Cabot received his MS from the University...
Get your 5 FREE Cloud Assemblies! What is "Cloud Assemblies"? It’s a new service you...
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