PanCanSeekTM
Hematologic Malignancies Precision Diagnosis and Therapeutics Guidance Test
PanCanSeek™ utilizes whole-genome sequencing (50×) of bone marrow cell DNA to offer comprehensive genomic profiling. By capturing four types of genomic variants, including structural variants (SVs), copy number aberrations (CNAs), copy number neutral loss of heterozygosity (CN-LOH), and single nucleotide variations (SNVs and InDels), this approach enables clinicians to conduct accurate molecular typing, effective prognostic stratification, and precise therapeutic guidance.
One for All
PanCanSeekTM, one test to detect four types of genetic variations across the entire genome.
How it works
Customer order
Customers can place orders through SeekIn official website or local agents
Blood-draw
2ml bone marrow collected in EDTA tubes and ransport under refrigeration
Testing
Detection by next generation sequencing (NGS) platform
Reporting
The test results will be ready in about 15 workdays after your blood draw arrived at central lab
