Detection of copy number variation from low-coverage whole-genome sequencing data
Zuzana Klinovská, Marcel Kucharik, Martina Sekelská, Michaela Hýblová, Jaroslav Budiš, Tomáš Szemes
Copy number variation (CNV) is a form of structural variant that leads to an abnormal number of copies of genomic regions in a cell. Next-generation-sequencing...
Breast cancer encompasses heterogeneous group of tumors with different histological, biological and clinical behavior. Intra- and inter-tumor heterogeneity as a result of genetic and non-genetic...
