This site is still under development. Information, features, and some organizational
aspects of the data still need further work and will change as we continue building.

WGS

Hover over a term you want explained. If you need more details, then click on the term and a new tab will open with a full details page.

What Whole Genome Sequencing Means in Everyday Medical Language

Whole Genome Sequencing, often called WGS, is a laboratory method that reads the exact order of all the DNA building blocks in a person’s genome. The genome is the complete set of genetic instructions found in every cell. By reading this entire sequence, doctors and researchers can look for changes or mutations that might cause diseases, including cancer.

WGS is sometimes called full genome sequencing or simply genome sequencing. It provides a very detailed picture of a person’s DNA, beyond what simpler genetic tests might show.

Why Whole Genome Sequencing Can Matter in Cancer Care

In cancer care, WGS can help identify genetic changes in tumor cells that might explain how the cancer started or behaves. This information can sometimes guide doctors in choosing treatments or understanding the risk of the cancer coming back. However, WGS is just one piece of the puzzle and is usually combined with other tests and clinical information.

What Patients Might See or Hear About WGS

Patients may encounter the term WGS in educational materials, medical reports, visit notes, or treatment discussions. Because the term can appear in different ways, such as “Whole Genome Sequencing,” it’s helpful to compare the wording and ask your care team to clarify what it means for your specific case.

Seeing the term WGS does not mean you have a diagnosis or that a particular treatment is planned. It means that a detailed genetic test was done or considered, and the results need to be interpreted carefully by your healthcare providers.

Common Confusions and How to Understand WGS in Context

WGS is a complex test, and its results can be complicated. It’s important not to overinterpret the term alone. For example, finding a genetic change does not always mean it causes disease, and not finding one does not guarantee there is no risk.

Because WGS may be called by different names or appear in various reports, patients should ask their care team to explain what the test results mean for their health and treatment options. This helps avoid confusion and ensures the information is used appropriately.

Next Steps and Safety Information

This explanation is for education only and does not decide what is safe or appropriate for any individual. If you see WGS mentioned in your medical records or hear it during your care, the best next step is to ask your healthcare team to explain what it means in your specific situation. They can help you understand how the test results fit into your diagnosis, treatment plan, or follow-up care.

Remember, WGS is a tool that provides information. Your care team uses this information along with other tests and your overall health to guide decisions. Always feel comfortable asking questions to make sure you understand what WGS means for you.

Sources

Public source information used for this glossary entry includes: