Genome analysis has led to a new era of precision medicine. Disease-related genetic alterations can now be detected in DNA fragments circulating in the bloodstream.
All cells shed DNA creating a tremendous opportunity for non-invasive disease detection. A single blood draw can reveal a person’s genetic predisposition to disease or even specific drug therapies. But deep knowledge requires powerful tools and precision is paramount to uncovering the genetic clues floating in our blood. We are developing novel genomic tools to reveal DNA alterations with unprecedented accuracy for clinical and research use.
Our team is passionate, experienced and looking to expand.
Avida Biomed presented Point-N-Seq, our new liquid biopsy NGS solution at ASCO on May 29th, 2020. Point-n-Seq is the first technology that can conduct a combined methylation and genomic alteration analysis without having to split samples. With an analytical sensitivity of 0.003%, a turnaround time of just 2 days at 1/5th of the sequencing cost, Point-n-Seq is a higher performing, more cost-effective technology poised to fill the gaps in existing NGS solutions. Results from our pilot study analyzing plasma collected from CRC patients and individuals with polyps suggest that Point-n-Seq is the ideal platform solution for screening and monitoring cancer at-scale.
May 29-31, 2020 Virtual Meeting
Avida Biomed to present promising performance data for its novel targeted methylation sequencing technology, Point-n-Seq, and pilot study of detecting early-stage cancer with plasma cfDNA at the 2020 American Association annual meeting for Cancer Research in San Diego
Session Category: Prevention Research
Session Title: Late-Breaking Research: Prevention, Early Detection, and Interception
June 22- 24, 2020
Virtual Meeting II, Sessions Available Online
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