Omics Services
Clinical Capabilities
The right treatment. The right patient. The right time. Learn more about precision medicine with Psomagen.
Our Clinical Services
Genetic Testing
Whether you are looking for prenatal testing, want to know your risk for heritable cancers or rare diseases, or need genetic testing for cardiac, kidney, or neuropsychological conditions, trust Psomagen’s precision medicine team to deliver actionable results.
Psomagen's extensive list of genetic panels offer diverse screening options.
Prenatal Panels
Expanded Carrier Screening
401 genes
ACOG/ACMG Female Carrier Screening
15 genes
Female Carrier Screening
30 genes
Cardiac NGS Panels
Cardiomyopathy
129 genes
Arrhythmia
76 genes
Kidney NGS Panels
Polycystic Kidney Disease
59 genes
Renal/Urinary Cancer
28 genes
Neuropsychological NGS Panels
Epilepsy
24 genes
Parkinson's / Alzheimer's / Dementia
35 genes
Hereditary Cancer Panels
Hereditary Disease
41 genes
Breast
20 genes
Breast / Ovarian
25 genes
Ovarian
19 genes
Colorectal
22 genes
Endometrial 1
11 genes
Gastric
15 genes
Pancreatic
22 genes
Hematologic Malignancy
16 genes
Melanoma
14 genes
NS / Brain
27 genes
Prostate
12 genes
Paraganglioma-Pheochromocytoma
11 genes
Sarcoma
26 genes
Thyroid
7 genes
ACMG Panels
Incidental Findings Gene Panel
81 genes
Additional Services
Sanger Sequencing
Sanger sequencing is the gold standard sequencing method, used to sequence polymerase chain reaction (PCR) products, plasmid DNA, and bacterial artificial chromosomes (BACs). At Psomagen, our well-trained team can use this method as confirmation of results you have received, or as stand alone testing in some cases.
Sanger sequencing is useful as a low-cost, high accuracy method for interrogating small DNA regions in a limited number of samples.