NIPT Gender is the simplest version of the NonInvasive Prenatal Test (NIPT), designed for parents who primarily want to know their baby’s sex early in pregnancy.
NIPT Basic is the entrylevel NonInvasive Prenatal Test designed to screen for the most common chromosomal conditions in pregnancy.
NIPT Standard is a more comprehensive version of the NonInvasive Prenatal Test, designed for parents who want deeper insights into their baby’s chromosomal health.
NIPT Plus is an advanced version of the NonInvasive Prenatal Test (NIPT) designed to give expecting parents the most comprehensive view of their baby’s chromosomal health.
Covers breast, ovarian, colorectal, prostate, pancreatic, gastric, melanoma, endocrine, and more.
BRCA1/2 and related genes for breast and ovarian cancer risk.
Genes linked to inherited prostate cancer risk.
Genes associated with inherited pancreatic cancer risk.
Genes for Lynch syndrome and other colorectal risks.
Every cancer is unique. Whether it’s prostate, breast, lung, liver, ovarian, or pancreatic cancer, the best outcomes come from understanding the genetic drivers behind each tumor.
At Direct by Syndicate Bio, we use advanced genomic profiling to uncover the mutations fueling cancer growth. This transforms care—moving beyond one-size-fits-all approaches to deliver actionable insights and targeted therapies tailored to each patient.
This approach is reshaping how we treat cancers of the prostate, breast, lung, liver, ovary, and pancreas, as well as myeloid cancers—helping patients access therapies that are more effective and less toxic.
Genetic profiling can reveal mutations that open the door to life-changing therapies, such as:
Androgen receptor–targeted therapies guided by AR-V7 or DNA repair mutations.
HER2-directed therapies or PARP inhibitors for BRCA1/2 mutations.
EGFR, ALK, and KRAS G12C inhibitors for targeted precision therapy.
Biomarker-driven immunotherapy for MSI-High or PD-L1 positive tumors.
PARP inhibitors for BRCA mutations and HRD-positive tumors.
Targeted therapy for KRAS, BRCA, or mismatch repair deficiencies.
FLT3, IDH1/2, and NPM1 mutations guiding targeted inhibitors; TP53 and complex karyotype markers informing prognosis and treatment intensity.
Direct by Syndicate Bio is committed to making cutting-edge genomic testing accessible across Africa. By integrating OncoMap50 for solid tumors and OncoMap90 for myeloid cancers into cancer care, we empower both patients and healthcare professionals to make smarter, faster, and more effective treatment decisions.
Genetic profiling is a test that looks at the DNA of a tumor or blood cancer to identify mutations that may be driving its growth. These insights help doctors choose treatments that specifically target those mutations.
By understanding the genetic makeup of a tumor or blood cancer, doctors can recommend therapies that are more likely to work—such as targeted drugs or immunotherapies—rather than relying only on standard chemotherapy.
Genomic testing is valuable across many cancers, including prostate, breast, lung, liver, ovarian, pancreatic cancers, and myeloid cancers like AML and MDS.
OncoMap50 analyzes 50 key genes in solid tumors and is ideal for patients starting targeted therapy.
OncoMap90 covers 90 genes relevant to myeloid cancers, offering a comprehensive view for blood cancers such as AML and MDS.
Yes. Many patients who don’t respond to standard therapies discover new treatment options or clinical trials through genetic profiling.
Yes. Direct by Syndicate Bio is dedicated to making precision oncology accessible across Africa, ensuring patients and healthcare providers can benefit from world-class genomic insights.
Because every cancer is different, treatment should be too.
Ask your doctor if OncoMap50 (solid tumors) or OncoMap90 (myeloid cancers) can guide your cancer treatment.
Partner with us to bring precision oncology to your patients.
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