BGI is dedicated to utilizing genomics in order to advance precision medicine for cancer. BGI’s next-generation sequencing essays offer a variety of options, including targeted panels that analyze genes directly linked to specific cancers by well-documented scientific research, and also much larger cancer panels designed for cancer analysis and discovery.
BGI’s cancer panels are designed to identify all four classes of actionable genomic alterations, including base substitutions, insertions and deletions, copy number alterations, and selected fusions. Both tissue samples and liquid biopsy samples are supported.
BGI’s lung cancer panel covers 20 genes（or 13 genes while using ctDNA） with direct therapeutic implications for 42 targeted drugs, including those recommended in the latest NCCN guidelines. The panel detects all classes of genomic alterations including SNV, CNV, InDels, and Fusion using routine FFPE samples, tumor tissue, biopsy, DNA, or peripheral blood.
Patients identified as having lung cancer
Tissue - Fresh/Frozen Tumor tissue, biopsy, FFPE, DNA. ctDNA - Peripheral blood (10mL)
Target region capture, High-throughput sequencing
Ordering the BGI SENTIS™ Lung Cancer Panel is easy.
Physician orders test
Blood or saliva sample collected
Sample shipped to BGI and analyzed
Results sent to physician