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Global leader in genomic diagnostics partners with Accuracy Plus to advance rare disease detection
GeneDx is expanding access to advanced genetic testing with fast, precise, and clinically actionable insights backed by over 25 years of expertise.
Accuracy Plus Medical Laboratory has collaborated with GeneDx to bring these services closer to patients and healthcare providers, enabling earlier and more accurate diagnoses.
With nearly one million exomes and genomes analyzed, GeneDx continues to enhance diagnostic accuracy and support better patient outcomes through early detection.
Many conditions share similar symptoms but have different genetic causes. Exome and genome testing analyze over 20,000 genes, improving the chances of finding the root cause early.
Key benefits:
• Accurate diagnosis
• Personalized treatment plans
• Better understanding of disease progression
• Access to support resources
Nearly 80% of rare diseases have a genetic origin, making comprehensive testing essential.
Exome testing analyzes the part of your DNA responsible for producing proteins. Since most known genetic conditions are linked to changes in this region, exome testing is highly effective in identifying potential genetic causes.
Genome testing examines genetic variations across your entire DNA, offering a more comprehensive analysis. Your healthcare provider can help determine whether you or your child may benefit from this broader level of testing.
IMBdx is a pioneer in liquid biopsy innovation, with global recognition for its AlphaLiquid platforms and CancerFind™️ technology. They are KOSDAQ-listed and accredited by top international bodies (e.g., CAP, ISO 13485), underscoring their commitment to precision, quality, and innovation.
By integrating IMBdx’s advanced testing solutions, APML reaffirms its commitment to delivering world-class diagnostics and empowering healthcare professionals with the tools they need for more informed, impactful cancer care.
Leading medical bodies recommend exome and genome testing as first-line diagnostics:
• American College of Medical Genetics and Genomics: Developmental delays, intellectual disabilities, congenital anomalies
• National Society of Genetic Counselors: Unexplained epilepsy (endorsed by American Epilepsy Society)
• American Ac
Comprehensive Genetic Insights for Early Answers
Exome and genome testing analyze over 20,000 genes, helping identify genetic causes quickly
and accurately. Recommended by leading bodies like the American College of Medical Genetics
and Genomics and National Society of Genetic Counselors, they improve early diagnosis—
especially as nearly 80% of rare diseases are genetic.
Whole Exome Sequencing (WES) is an advanced genetic test that helps diagnose a wide range of rare and inherited conditions, including:
How do DNA, chromosomes, genes, and proteins work?
• DNA: The body’s instruction guide
• Chromosomes: Organized sections of DNA
• Genes: Instructions for making proteins
• Proteins: Essential components that build and run the body
What is a genetic variant?
A genetic variant is a change in a gene that may affect how the body develops or functions. Genetic testing helps identify these changes and guide care.
Exome and genome testing provide a comprehensive view of your child’s genes, helping uncover potential genetic causes sooner.
Contact Accuracy Plus Medical Laboratory to learn if these advanced tests may be appropriate for your child.
At Accuracy Plus, we create a scientific, all-inclusive, and value-adding diagnostic culture of excellent, timely test results conforming to world-class testing standards and benchmarks for swifter and better disease detection.
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