Unknown Genetic Disorders

Test for Unknown Genetic Disorders

Whole Genome Sequencing

Whole genome sequencing identifies almost all changes in a patient’s DNA by sequencing both the entire coding and non-coding regions of the genome. CentoGenome® – our whole genome sequencing service – is the most complete solution to diagnose genetically complex and undiagnosed cases with the highest level of certainty.

CentoGenome®

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CentoGenome®is the most complete solution to diagnose genetically complex and undiagnosed cases with the highest level of certainty.

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Whole Exome Sequencing

Clinical Exome Sequencing is a test for identifying disease causing DNA mutations in the protein coding (exon) regions of the human genome. Along with the patient’s clinical presentation and other known disease markers, Clinical Exome Sequencing provides a powerful means by which genetic disorders can be uncovered in an individual – leading to more informed approaches for personalized care and treatment.

CentoXome®

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CentoXome® is the best choice when you need a fast, accurate, and cost-effective one-step solution to complete the diagnostic process of complex and unsolved cases.

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