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Bio B2BACT Genomics 〉Hereditary Risk Evaluation

Hereditary Risk Evaluation

Hereditary Risk Evaluation

Most powerful in hereditary risk evaluation.
NGS panel design of 32 genes and provide medical report in 30 calendar days.

Request for Collaboration
Overview
ACTRiskTM  Hereditary Risk Evaluation is used to examine hereditary cancer related genetic alterations for people with risk of hereditary cancer. 
Using next generation sequencing (NGS) to test 32 genes, ACTRiskTM helps physicians and genetic counselors to precisely evaluate cancer risk and discuss risk management options with high-risk individuals.
 
Features
  • Most powerful in hereditary risk evaluation
  • NGS panel design of 32 genes
  • AI-powered bioinformatics analysis of cancer genetic mutations of SNV & Indel and splice site variants
  • High-quality test result in CAP-certified lab
  • Turnaround time with 30 calendar days  
Specifications
  • Next Generation Sequencing : 32 genes
  • NGS Sequencing Mean Depth: >500 X
  • Sample Types :  8 ml whole blood
Application
  • Individuals with a family history of cancer
  • Cancer patients with a family history of cancer
  • Cancer patients without family history of cancer but have multiple tumors diagnosed before age 50
  • Individuals highly concerned with risk of hereditary cancer
Collaboration Options
  • Clinical Services : Provide cancer genomic profiling to enable personalized treatment plan.
  • Biomarker Discovery : We provide comprehensive cancer genomic profiling to facilitate biomarker discovery. Customized assay is available.
  • Patient Stratification : From next generation sequencing, IHC and PCR assay, we utilize various platforms to screen patients prospectively.
  • Consultation : Our team of industry veterans and in-house clinical database offer insights to ensure smooth clinical trial operations.
  • CDx Development : We offer companion diagnostic development on NGS-based or CHIP-based multiplex qPCR platforms.
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