Custom Solutions for RNA and DNA-Sequencing in Cancer Research
Credit: iStock
Next-generation sequencing is a key technique used in cancer research and diagnostics. However, obtaining reliable data from complex samples, including delicate formalin-fixed paraffin-embedded (FFPE) tumor samples, can be challenging.
In this application note, clinical scientists explain how they optimized their genomics testing methods, using custom targeted DNA- and RNA-sequencing panels, to attain reliable fusion data from FFPE samples.
Download this application note to discover:
- An optimized library preparation process to improve key sequencing quality metrics
- Software to develop custom panels for identification of solid tumors
- A high-quality RNA kit to improve the reliability of library preparation
Brought to you by
Download This App Note for FREE Now!
Information you provide will be shared with the sponsors for this content. Technology Networks or its sponsors may contact you to offer you content or products based on your interest in this topic. You may opt-out at any time.
