The use of whole genome sequencing in breast cancer research has significantly advanced our understanding of the disease. By analyzing the complete DNA sequence of breast cancer tissues, scientists can identify unique genetic mutations and variations. This detailed genetic information enables the development of personalized treatment plans, tailoring therapies to the specific genetic makeup of an individual’s cancer, thereby improving outcomes and reducing side effects.
![](/sites/default/files/default_images/Women%20in%20Tech%20profile%20picture.png)
- Log in or register to contribute
Contribute to three or more articles across any domain to qualify for the Contributor badge. Please check back tomorrow for updates on your progress.