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GTR Home > Tests > NeoTYPE® Discovery Profile for Solid Tumors


Test name


NeoTYPE® Discovery Profile for Solid Tumors

Purpose of the test


This is a clinical test intended for Help: Prognostic, Therapeutic management



Click Indication tab for more information.

How to order


Order URL Help: https://www.neogenomics.com/test-menu/neotype-discovery-profile-solid-tumors

Specimen source

Paraffin block


Biochemical Genetics
Protein Expression
FFluorescence in situ hybridization (FISH)
Fluorescence in situ hybridization (FISH)
Molecular Genetics
CSequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)

Summary of what is tested

Click Methodology tab for more information.

Clinical utility


Guidance for selecting a drug therapy and/or dose

  • The NeoTYPE™ Discovery Profile for Solid Tumors is a 326 test profile that combines NGS, FISH and IHC to allow for the accurate and sensitive detection of genomic alterations in the genes most relevant to various solid tumor cancers. These genomic alterations include SNP's, indels, rearrangements and other alterations. Testing can aid in the diagnosis of various diseases and provide information to develop strategies for the treatment and management of the underlying disease. In addition, the results obtained from the NeoTYPE™ Discovery Profile for Solid Tumors can also be used in current or future clinical research projects.

Clinical validity


Not provided

Test services

  • Clinical Testing/Confirmation of Mutations Identified Previously
  • Pharma Services
  • Result interpretation

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.