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In cancer research, NGS is often used to identify genetic variations and mutations. Researchers and clinicians use NGS to look at large portions of DNA and RNA at once. Then, they identify any abnormalities that could be related to the disease.
Molecular Profiling of Solid Tumors Next-generation sequencing (NGS) provides a comprehensive method for assessing the majority of genes associated with solid tumors, including lung, colon, breast, melanoma, gastric, and ovarian cancers.
Molecular Profiling of Solid Tumors Next-generation sequencing (NGS) provides a comprehensive method for assessing the majority of genes associated with solid tumors, including lung, colon, breast, melanoma, gastric, and ovarian cancers.
Listen to pronunciation. (SAH-lid TOO-mer) An abnormal mass of tissue that usually does not contain cysts or liquid areas. Solid tumors may be benign (not cancer), or malignant (cancer).
The Solid Tumor Profile is designed to analyze the molecular abnormalities of DNA in various solid tumors including cancers of the lung, pancreas, brain, colon, breast, ovary, endometrium, thyroid, head and neck, and soft tissue (sarcoma and GIST).
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Genomic tumor profiling by next-generation sequencing (NGS) allows for large-scale tumor testing to inform targeted cancer therapies and immunotherapies, and to identify patients for clinical trials.

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