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Whole Exome Sequencing | WES DUO and TRIO

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The Whole Exome is the most common genetic test used to identify variants in a person’s genetic data that may be associated with a disease or developmental process.  With the use of Next-Generation Sequencing technology, the technology exists for rapid and cost-effective genetic testing.

Whole Exome Analysis Only

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Whole Exome Sequence Analysis ONLY

Many companies provide Whole Exome Analysis.  We are experts in this, using the most advanced in ai based bioinformatics, we can analyze WES raw data generated from other laboratories, provided the data is in the appropriate format.

Contact us to make sure in advance.

Comprehensive Genetic Insights: Autism and Intellectual Disability Testing

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Uncover the genetic foundations of autism and intellectual disability with our groundbreaking Next-Generation Sequencing (NGS) Genetic Test. This state-of-the-art test represents a significant leap in medical technology, offering a deeper understanding of the genetic factors influencing these complex conditions.

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Genetic Cardiovascular Disease Panel

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NGS Genetic Cardiovascular Disease Panel consists of testing for more than 300 genes associated with genetic neurological disease/disorders.  Our panel looks for genes associated with the most common cardiovascular diseases with a genetic component.

We use an advanced AI-driven bioinformatics pipeline that includes searches across 50+ databases including a 750000-person genetic disease database.

Genetic Comprehensive Cancer Panel

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NGS Genetic Comprehensive Cancer Panel consists of testing for more than 100 genes associated with genetic cancer risk predispositions.  Our panel looks for genes associated with in increased risk of developing cancer in an individual or their family.  Testing strategy may involve testing other family members or affected family members first

We use an advanced AI-driven bioinformatics pipeline that includes searches across 50+ databases including a 750000-person genetic disease database.

Genetic Neurological Disease Panel

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NGS Genetic Neurological Disease Panel consists of testing for more than 1900 genes associated with genetic neurological disease/disorders.  Our panel looks for genes associated with the most common neurological diseases with a genetic component.

We use an advanced AI-driven bioinformatics pipeline that includes searches across 50+ databases including a 750000-person genetic disease database.

Genetic Skin Disease Panel

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NGS Genetic Skin Disease Panel consists of testing for more than 160 genes associated with genetic skin disease/disorders.  Our panel looks for genes associated with the most common hereditary skin diseases.

We use an advanced AI-driven bioinformatics pipeline that includes searches across 50+ databases including a 750000-person genetic disease database.

Whole Exome Sequencing | WES

Sold: 0

The Whole Exome is the most common genetic test used to identify variants in a person’s genetic data that may be associated with a disease or developmental process.  With the use of Next-Generation Sequencing technology, the technology exists for rapid and cost-effective genetic testing.

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