---
title: The Power of Discovery
image: https://viewonline.the-scientist.com/hubfs/downloads/TS/TS_Qiagen/TS_PPL_Qiagen_QCI_App%20Note/1800x640.jpg
---

 APPLICATION NOTE

![Qiagen Logo on 393939](https://viewonline.the-scientist.com/hubfs/downloads/TS/TS_Qiagen/TS_PPL_Qiagen_QCI_App%20Note/Qiagen%20Logo%20on%20393939.jpg "Qiagen Logo on 393939")

# The Power of Discovery

## Harnessing insights into heritable mutations from whole-exome sequencing data

Whole-exome sequencing (WES) specifically targets thousands of protein-coding regions of the genome, offering an affordable and efficient approach for detecting rare genetic variants and discovering disease biomarkers. To identify the relevant genetic variations contributing to a phenotype and symptoms, researchers employ software solutions, such as QCI Interpret Translational, to simplify and accelerate the genomics data analysis process by eliminating manual curation.

### Download this application note from QIAGEN to learn about a robust WES workflow for rapid variant annotation, filtering, and triage.

- Explore how WES discovers novel genes and variants
- Learn how to overcome challenges in high-throughput WES data analysis
- Discover the value of automated, evidence-powered variant filtering and prioritization when handling WES data for hereditary cancer research

## Download the WES Application Note Now

![473x300 Tablet on FFFFFF](https://viewonline.the-scientist.com/hs-fs/hubfs/downloads/TS/TS_Qiagen/TS_PPL_Qiagen_QCI_App%20Note/473x300%20Tablet%20on%20FFFFFF.jpg?width=473&height=303&name=473x300%20Tablet%20on%20FFFFFF.jpg "473x300 Tablet on FFFFFF")

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