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…
Is Open Source NGS Software for You?
An interview with Eric Cabot Ph.D. Dr. Eric Cabot received his MS from the University...
Q&A: NGS Sequence Assembly on the Cloud
Get your 5 FREE Cloud Assemblies! What is "Cloud Assemblies"? It’s a new service you...
Free NGS Assembly and Alignment for Genomic Sequencing Data
We know that for many researchers, performing large scale next-generation sequence alignments or de novo sequence assemblies on their computers can be a problem due to insufficient hard disk space or memory.
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