Ontology highlight
ABSTRACT: Background
The study of cancer genomics continually matures as the number of patient samples sequenced increases. As more data is generated, oncogenic drivers for specific cancer types are discovered along with their associated risks. This in turn leads to potential treatment strategies that pave the way to precision medicine. However, significant financial and analytical barriers make it infeasible to sequence the entire genome of every patient. In contrast, targeted sequencing panels give reliable information on relevant portions of the genome at a fiscally responsible cost. Therefore, we have created the Targeted Panel (TarPan) Viewer, a software tool, to investigate this type of data.Results
TarPan Viewer helps investigators understand data from targeted sequencing data
SUBMITTER: Ashby C
PROVIDER: S-EPMC7158102 | biostudies-literature | 2020 Apr
REPOSITORIES: biostudies-literature