Methods and compositions for treating melanoma
US-2024424002-A1 · Dec 26, 2024 · US
US10072298B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10072298-B2 |
| Application number | US-201514672066-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 27, 2015 |
| Priority date | Apr 17, 2013 |
| Publication date | Sep 11, 2018 |
| Grant date | Sep 11, 2018 |
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The disclosure provides gene fusions, gene variants, and novel associations with disease states, as well as kits, probes, and methods of using the same.
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What is claimed: 1. A method of detecting a CEP85L-ROS1 gene fusion in a sample from a subject, the method comprising: generating a reaction mixture comprising nucleic acid from the sample and a pair of primers that specifically hybridize to a target nucleic acid comprising the sequence of SEQ ID NO:17 , wherein the sample comprises the target nucleic acid; amplifying the target nucleic acid using the pair of primers, thereby producing amplicons; sequencing the amplicons; and detecting the presence of a CEP85L-ROS1 gene fusion comprising the sequence of SEQ ID NO:17 in the sequenced amplicons. 2. The method of claim 1 , further comprising diagnosing the subject as having glioblastoma and determining a treatment based on the CEP85L-ROS1 gene fusion detected in the sample. 3. The method of claim 2 , wherein the treatment is crizotinib. 4. The method of claim 1 , wherein the sample is a blood sample. 5. The method of claim 1 , wherein the sample is a tissue sample. 6. The method of claim 5 , wherein the sample is a formalin-fixed, paraffin-embedded sample. 7. The method of claim 1 , wherein the sample comprises tumor tissue. 8. The method of claim 7 , wherein the tumor is a glioblastoma. 9. The method of claim 1 , wherein the sequencing is by next generation sequencing technology.
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