Live Webinar on RNA-Seq Data Analysis on 28 Feb 2018
Strand NGS is a biologist friendly NGS analysis tool that allows biologists to analyze their data using a very intuitive workflow for the analysis and...
Is there a bias after DNA fragmentation? What do you think?
Cutting DNA into small fragments is a key preparation step for DNA sequencing with NGS technology. To reduce errors and increase reliability of the sequence...
Webinar on Fast and Accurate DNA Variant Calling on 26 Apr 2017
Presenting Strand NGS v3.0 best-practices: a DNA-Seq workflow that identifies highly accurate variants from raw reads. Our best practices workflow is...