TEST:

PanCanSeek®

PanCanSeek® is developed as the world's first integrated solution for leukemia cytogenetics and molecular diagnostics. It uses high-depth WGS, which can cover four different detection techniques – karyotyping for CNV, FISH for gene fusion, qPCR for single mutation and targeted NGS panel for multiple mutations. All the mutation information of the genome can be obtained from this single test, so that molecular typing, prognosis stratification, treatment guidance, and efficacy prediction can be performed faster, more accurately and more effectively. PanCanSeek® requires ~2ml bone marrow from leukemia patients for high-depth WGS (50x coverage) to detect all types of mutations including single nucleotide variants (SNVs), small insertion and deletion (InDels), copy number aberrations (CNAs), and structure variants (SVs). The test is intended to be used in molecular classification, prognosis stratification, treatment guidance, and efficacy prediction. PanCanSeek® Cancer Mutation Detection Kit is also suitable for patient who is suffering from complex leukemia by analyzing the genomic profiling result to explore the genetic causes of the disease and find the appropriate treatment strategies.