BXGWB WEBINAR
Webinar recordings
Fast and easy identification of disease causing variants in hereditary diseases
In this presentation, we will present our new one-step trio workflow, which...
Webinar recordings
RNA-Seq Solution: Analyze your RNA-seq data in Biomedical Genomics Workbench
In this webinar we show how to analyze paired tumor-normal samples from two cancers,...
Webinar recordings
Solving hereditary disease trios using bioinformatics solutions for clinical...
In this webinar Dr. Anika Joecker is going through the key features and benefits of our...
Webinar recordings
Getting started with Biomedical Genomics Workbench - Part 1
An introduction to Biomedical Genomics Workbench focusing on the basic features and how...
Webinar recordings
Rapid and highly accurate end-to-end NGS analysis solution for detection of...
Rapid and highly accurate end-to-end NGS analysis solution for detection of novel...
