Every day without a genetic diagnosis is a missed opportunity An earlier genetic diagnosis is proven to:4,5 Recommended as a first‑line test American College of Medical Genetics and Genomics recommends exome or genome as a first-tier test for developmental delay, intellectual disability, and congenital anomalies.15 Explore exome for pediatric developmental disorders National Society of Genetic Counselors … Exome Sequencing
Take a guideline-driven approach.Start with exome. *Fictionalized case study for illustrative purposes only References
With comprehensive care from start to finish, GeneDx offers more than a test result. Experience the GeneDx difference and help your patients find answers. COMMON QUESTIONS *Fictionalized case study for illustrative purposes only References
Equitable access to Exomes and Genomes. Ordered by whom? This debate-style session will provide a forum for the Medical Genetics and Genomics community to examine evidence and opinions that are both for and against the ordering of exome and genome sequencing by non-genetics healthcare professionals. The session will feature a moderator and a panel of … 2024 ACMG Annual Clinical Genetics Meeting
We are proud to be in-network with many commercial and government payors. In-network status may not apply for all health plan types, in all geographies, or for all health plan network products, so we encourage ordering providers and patients to check the health plan for provider network status ahead of services being rendered. Additionally, network … In-Network Insurance Contracts
When genetic testing identifies variant(s) in a patient, targeted variant testing may be indicated for family members. Targeted variant testing is less costly than diagnostic analysis of the whole gene or panel of genes. Additionally, in most cases targeted variant testing for pathogenic or likely pathogenic variant(s) will provide a straightforward “negative” or “positive” result. … Targeted Variant Testing
Benefits of Whole Genome Sequencing Whole genome sequencing (WGS), also called genome testing, examines a person’s entire genome, including the protein-coding regions (called exons) and the non-coding regions (called introns). As a result, it is the most comprehensive genetic testing option available and enables the greatest chance of uncovering a genetic diagnosis. The Power of … Whole Genome Sequencing
GeneDx delivers on our promise to provide genomic insights with a superior clinical product, supporting you to deliver the best care. Genetic Testing for Pediatric Neurodevelopmental Disorders Whole exome sequencing (WES) is a comprehensive, cost-effective option recommended for patients with conditions such as: Rapid Genetic Testing for Acutely & Critically Ill Neonatal& Pediatric Patients … Provider Overview
Important Information Regarding GeneDx Test Menu Changes The information below outlines details regarding GeneDx tests that will be discontinued effective March 04, 2024. We will continue to offer a robust genetic testing menu, and for a subset of the tests being discontinued, potential alternative tests have been identified to support you and your patients. Below … Test Menu Changes
Go Deeper, See More Extensive and flexible hereditary cancer testing options to aid in personalized medical management. A legacy of expertise Our expertise in hereditary cancer began over a decade ago, founded by cancer-focused genetic counselors and molecular geneticists who wanted to lead genetic testing in clinical oncology. Today, we’re known for our expertise utilizing … Hereditary Cancer Testing
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