Follow
SNV - Oncology panels
A single nucleotide variants (SNV) describe genetic alterations occurring in a single nucleotide (adenine [A], thymine [T], cytosine [C], or guanine [G]). When a SVP occurs in more than 1% of a population it is known as a single nucleotide polymorphism (SNP). Oncology panels that screen for SNVs in a patient's tumor to aid in optimizing personalized treatment options.
What's Popular in SNV - Oncology panels
OCT 21, 2020 | 10:15 PM
Comprehensive genomic profiling in clinical studies helps to detect clinically relevant cancer driver mutations using low amount of tumor tissues within several days. Recent studies have sho...
APR 10, 2019 | 10:30 AM
The BRCA1 and BRCA2 genes represent the best examples of the modern understanding of cancer molecular genetics. Testing for germline and somatic mutations in BRCA 1/2 has gradually become com...
APR 06, 2016 | 1:30 PM
Cancer remains the second leading cause of death in the United States. Most tumors arise from a myriad of genetic changes that dysregulate cell growth and prompt survival. Ident...
