Find the Right Path
Customize your cancer treatment to see better results. Let us decode the specific genomic causes of your cancer and recommend the optimal treatment plan for you.
Why ACT Genomics
High Success Rate
We achieve exceptional results with limited samples by continually optimizing our laboratory protocols.
In Sync Database
We ensure relevant clinical application in sync with periodically updated databases.
Timely, Ongoing Support
We offer test consultations and deliver speedy reports with 1-on-1 report consultations for ongoing support.
ACT Genomics is internationally recognized and engaged by major cancer hospitals and clinics.
Implement of next-generation sequencing (NGS) and multiplex molecular testing platforms, coupled with sophisticated bioinformatics analysis tools.
Our solid cases in clinical and research fields provides rich Asian-prone database to conduct precision bioinformatic analysis.
Thoughtful, Ongoing Support
By integrating above, ACT Genomics provides thoughtful and ongoing support to cancer treatment. Our team provides extensive cares to patients from bioinformatic, medical and nursing perspective.
How to Get Started
Your doctor will assess your medical history to determine if a genomic test is needed. Our genomic testing services are available only through a medical practitioner (doctor).
Once your doctor selects the appropriate genomic test, we will assist in collecting and sending your sample to our laboratory.
Upon receiving your sample, we will first conduct quality control. Once approved, the testing will take 8 to 21 working days depending on the ordered genomic test. We will send the results to your doctor.
At your next appointment, your doctor will explain the test results and discuss the most suitable treatment plan with you.