Using Lasergene to De Novo Assemble PacBio HiFi Data
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.
Master Viral Genome Analysis Webinar
Watch our 1-hour webinar on how to master viral genome analysis.
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 research?
Webinar: RNA-Seq Analysis using Lasergene Genomics
Watch our 1-hour webinar on best practices for aligning and analyzing RNA-Seq data using the…
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 Client…
Answers to your “Genomic Data Assembly Strategies” webinar questions
Check out our new post featuring questions and answers from our recent webinar on genomic…
How to Assemble Genomes like a Bioinformatics Pro
Whether you are working with Illumina, Oxford Nanopore, PacBio data, or a combination of these…
Webinar: Choosing the best assembly strategy for your genomic sequencing data
Watch our 1-hour webinar for an in-depth look at different assembly strategies for genomic sequencing…
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…
Working with Variant Call Format Files in Lasergene Genomics
DNASTAR’s Variant Annotation workflow provides functional annotation and enriched information for analyzing human samples in…
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