Our Services
Comprehensive genetic testing and counseling across 20 organ systems.
Diagnostic Genetic Testing
Our core service: identifying the molecular basis of suspected genetic conditions. We evaluate patients across all 20 organ systems using the most appropriate testing strategy for each clinical presentation.
- Unexplained symptoms across any organ system
- Family history suggestive of genetic condition
- Failed prior diagnostic workup
- Confirmation of clinical diagnosis
Rapid Critical Care Genomics
Time-critical genetic diagnosis for critically ill neonates and children. Rapid exome and genome sequencing delivers results in 3–7 days, when every hour matters.
- NICU: 34–59% diagnostic yield, 25% LOS reduction
- PICU/CICU: 31–59% yield, 80% management change rate
- 3–7 day turnaround for rapid sequencing
- Diagnosis within the admission, before the odyssey begins
Carrier Screening & Reproductive Genetics
Genetic evaluation for family planning, including carrier screening for prospective parents, prenatal genetic assessment, and reproductive decision support.
- Pre-conception carrier screening
- Prenatal genetic evaluation
- Cascade family testing
- Reproductive risk counseling
Pharmacogenomics
Genetic profiling to guide medication selection and dosing. Identify how your genetic makeup affects drug metabolism to optimize treatment and prevent adverse reactions.
- Medication response profiling
- Adverse event risk prediction
- Dosing optimization
- Multi-drug interaction assessment
Testing Methodologies
We select the right test for each clinical scenario based on evidence and indication.
Gene Panels
Targeted analysis of specific genes associated with a known clinical presentation. Best when the phenotype strongly suggests a specific group of conditions.
Turnaround: 2–4 weeks
Exome Sequencing
Analysis of all protein-coding regions of the genome (~20,000 genes). The most common comprehensive test for undiagnosed conditions.
Turnaround: 4–8 weeks
Genome Sequencing
Complete analysis of the entire genome, including non-coding regions. Captures structural variants and intronic changes that exome sequencing may miss.
Turnaround: 6–10 weeks
Rapid Sequencing
Expedited exome or genome sequencing for critically ill patients in intensive care settings where timely diagnosis directly impacts management.
Turnaround: 3–7 days
The CarePathways Approach
Every patient follows a structured diagnostic pathway from first contact to follow-up care.
Insurance & Coverage
Most genetic testing is covered by insurance when medically indicated. We work with all major insurance carriers and provide prior authorization support to ensure coverage before testing proceeds.
Typical testing costs range from $250 to $3,000 depending on the type of test ordered. Many patients have minimal out-of-pocket costs when testing is medically necessary.