Abstract Background Somatic copy number alternation (SCNA) is a common feature of the cancer genome and is associated with cancer etiology and prognosis. The allele-specific SCNA analysis of a tumor sample aims to identify the allele-specific copy numbers of both alleles. adjusting for the ploidy and the tumor purity. Next generation sequencing platforms produce abundant read counts a... https://citylocers.shop/product-category/swap-patch/