Prioritize 58 key genes if there's a family history indicating a potential hereditary link to cancer, like early-onset, rare, bilateral, or multiple primary cancers among family members.
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Dive into 79 genes for precise immunodeficiency diagnosis. Our streamlined platform fosters personalized treatment plans.
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Investigate 38 genes for precise diagnosis of Thyroid diseases, enabling early intervention and treatment to prevent complications or manage conditions more effectively.
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63 genes associated with specific neurological presentations. This program is available to individuals 18 or older suspected of or at risk of having neurology related genetic Diseases.
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Identifying variations in 48 genes related to endocrinology is crucial for early detection, allowing timely interventions to prevent complications or manage conditions effectively.
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Analyzing 98 genes aids in a comprehensive diagnosis, guiding prognosis, treatment selection, and potential qualification for therapies or clinical trials.
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The Cardiopulmonary Panel is designed to detect single nucleotide variants (SNVs)and small insertions and deletions in 63 genes associated with cardiopulmonary risk.
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Exciting News! Our newest product is on its way and we can't wait to share it with you!
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Exciting News! Our newest product is on its way and we can't wait to share it with you!
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It sequences over 500 genes known to be relevant to cancer treatment and assesses essential immunotherapy (IO) biomarkers, providing oncologists with a comprehensive view to devise tailored treatment plans for their patients. Genomic Testing that Change how Cancer will be Identified and Treated, Maximize Identification Of Molecularly Matched Therapies.
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Pharmacogenetics analysis reveals drug metabolism insights, aiding personalized medication choices and dosage adjustments based on individual genetic makeup.
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Read moreDownload FormThe test detects genetic material specific to Influenza A, B, and COVID viruses, aiding accurate diagnosis for these distinct infections.
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PCR COVID testing detects viral genetic material to diagnose infections accurately, crucial for identifying active cases with high sensitivity.
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The test identifies distinctive genetic sequences unique to the monkeypox virus. Extracting genetic material from a sample, like a swab, amplifies and detects these markers, ensuring precise diagnosis of monkeypox infection.
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