Secondary Analysis 2.0 – Part V
![Detection of CNVs](https://www.goldenhelix.com/blog/wp-content/uploads/2017/07/gene-1-176x176.jpg)
An Example of an Integrated Clinical Workflow for CNVs and SNVs In this blog series, I discuss the architecture of a state of the art secondary pipeline that is able to detect single nucleotide variations (SNVs) and copy number variations (CNVs) in one test leveraging next-gen sequencing. In Part I, we reviewed genetic variation in humans and looked at the key… Read more »