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BGI ServiceOverview SENTIS Cancer+Discovery

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Gain insight into clinically

actionable mutations and


discover new treatment targets
with one of the market’s most Introduction
comprehensive and affordable
Technological advances combined with
panels. improved understanding of the genetic basis of
cancer has revolutionized the way we manage
cancer. Utilizing patient’s particular genomic
profile, clinicians can now assess the risk of
hereditary cancer for the patient and patient’s
family, as well as tailor the best treatment
options.

BGI’s SENTIS™ Cancer+Discovery provides


clinicians with one of the market’s most
comprehensive and accurate Next Generation
Sequencing (NGS) based testing solution for the
identification of clinically actionable mutations,
as well as discovery of novel variants with
important function in cancer. Supporting both
tissue sample and liquid biopsy, the panel offers
whole exon coverage of 688 cancer-related
genes and interrogates most common types of
alterations including SNVs, indels, CNVs and
fusions in solid tumors.

The Power of Knowing


BGI SENTIS™ Cancer+Discovery (Tissue/ctDNA)

Advantages
Comprehensive - Whole exon coverage of 688 cancer-related genes, supporting most common types of genomic alterations
including base substitutions, InDel, CNV, fusion,TMB and MSI
- Includes genes associated with both sporadic and hereditary cancers
- Provides interpretation on the therapeutic relevance in 200+ drugs, including 260 targeted therapies (both
approved and currently in clinical trial), 11 immunotherapies and 11 commonly used chemotherapies
- Includes 425 genes in cancer-related pathways for discovery of novel pathogenic variants

Flexible - BGI SENTIS™ Cancer+Discovery (Tissue): matched fresh tissue, biopsy, FFPE, DNA and peripheral blood
- BGI SENTIS™ Cancer+Discovery (ctDNA): peripheral blood or DNA

Reliable - See technical information for details.

Liquid biopsy version allows genetic profiling in situations where tissue is not available or continuous monitoring
of tumor molecular profile is required.
The Power of Knowing
BGI SENTIS™ Cancer+Discovery (Tissue/ctDNA)

Gene Panel Overview Workflow

Counselling and
Colon
Pancreatic MSI 182 Interpretation Consent
carcinoma Therapy for more than
Cancer
Target Genes 200 drugs Sample Collection
Breast
Cancer DNA Extraction
Ovarian 63 Evaluate and QC
Cancer 688 Hereditary the risk for Targeted Capture
Cancer herediatary
Hepatobiliary
carcinoma
genes Genes cancer
and NGS
Gastric
Cancer
Data Analysis and
425 Discover Interpretation
Cancer genes potentially
Prostate Lung TMB Pathway important in drug Report Ready
Cancer Cancer Genes target and
resistance
Genetic Counselling

Technical Information

SENTIS Cancer+Discovery(Tissue) Limit of Detection(LoD) Positive Predicttive Value(PPV) Sensitivity

Single Nucleotide Variations(SNV) 1% 100% 99.2%

Indels 0.5% 93% 97.8%

Copy Number Amplifications(CNV) 3.4 copies 100% 100%

Splice Variants(SV) 0.5% 100% 100%

SENTIS Cancer+Discovery(ctDNA) Limit of Detection(LoD) Positive Predicttive Value(PPV) Sensitivity

SNV 0.6% 97.30% 98.3%

Indels 0.59% 100% 100%

CNV 3.5 copies 100% 100%

SV 1.25% 100% 100%

Sample Requirements Ordering Information


BGI SENTIS™ Cancer+Discovery (Tissue)
ITEM CATALOG NO.
- >60mg tissue or 15 FFPE 10mm*10mm (5-10µm) sections or ≥3 samplings of
biopsy or ≥3µg good quality, tumor DNA; BGI SENTIS™
- 5mL of peripheral blood Cancer+Discovery DX0643
(Tissue)
BGI SENTIS™ Cancer+Discovery (ctDNA) BGI SENTIS™
- ≥10mL of peripheral blood (separated plasma and formed elements) or ≥8mL of Cancer+Discovery DX0644
peripheral blood collected in Streck Cell-Free DNA BCT® tube (ctDNA)

Turnaround Time
Contact your local BGI representative for more information or email
20 days (from sample arriving at BGI lab to
info@bgi.com. More information can also be found on our website. report)
www.bgi.com/global/

Copyright© 2020 BGI. The BGI logo and SENTIS logo are trademarks of BGI. All rights reserved. Published January 2020, version 1.0
For Research Use Only. Not for use in diagnostic procedures.
Testing services not currently available in the United States of America. Please contact a representative for regional availability.

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