Advancing Rare Disease Diagnosis. One Innovative Test at a Time.

Going Beyond Traditional Testing Methods

Greenwood Genetic Center offers one of the most comprehensive and cutting-edge diagnostic test menus in medical genetics. Whether you're looking to expand your diagnostic toolkit or find answers for complex cases, we're here to support you and your patients.

Innovative Diagnostics Designed for Complex Cases

From epigenetic profiling to structural variant detection, our test menu is built to give clinicians and labs the answers they need.

  • Complete Optical Genome Mapping

    Detect a broad spectrum of structural variants with unmatched resolution. Ideal for cases where traditional cytogenetics falls short.

  • Targeted Optical Genome Mapping

    A focused approach to structural variant analysis when a specific region or condition is already suspected.

  • FSHD1 Optical Genome Mapping

    Purpose-built for Facioscapulohumeral Muscular Dystrophy diagnosis. Delivering precision where it matters most.

  • EpiSign Complete

    A genome-wide methylation analysis that identifies episignatures associated with rare neurodevelopmental and overgrowth syndromes.

  • EpiSign Variant

    Resolve variants of uncertain significance using epigenetic profiling. Designed to support clinical decision-making with greater confidence.

  • Disorders of Somatic Mosaicism Panel

    Detect low-level mosaic variants across a curated gene panel. Expanding diagnostic reach for conditions often missed by conventional testing.

  • Rapid Whole Genome Sequencing

    Fast, comprehensive genomic analysis for critically ill patients where time is a critical factor in diagnosis and treatment.

  • Whole Genome Sequencing

    The gold standard for undiagnosed rare disease. Broad coverage, deep insight, and expert interpretation.

Going Beyond Traditional Testing Methods

"Experts in medical genetics. Committed to diagnostic innovation."

Reuben has been part of the GGC family for nearly all of his life! He was diagnosed with propionic acidemia as an infant and receives life-saving care from GGC’s metabolic treatment team Dr. Schroer, Mitzi, and Dr. Burns. Reuben lights up our office every time he visits!

More Than a Lab. A Diagnostic Partner.

Innovative Test Menu

We continuously expand and refine our offerings to stay at the forefront of medical genetics diagnostics.

Expert Support

Our team of medical geneticists, genetic counselors, and lab scientists are available to help you navigate complex cases and select the right test.

Comprehensive Patient Care

From test selection to result interpretation, we work alongside you to ensure your patients get answers.

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Learn more about our genetic tests and download material American College of Medical Genetics & Genomics.


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