GeneSpect™ Reports: Automated NGS Data Interpretation
Thursday, November 21, 2024
3:45 PM – 4:15 PM PST
Location: Innovation Spotlight Stage #1
Labs employing NGS-based assays experience a common bottleneck: lack of resources, or lack of simple-to-execute tools to interpret the data for their clinician stakeholders. Intelliseq’s iFlow platform addresses this problem through its cloud-based fully automated workflows, either pre-built or fully customized. Medical Director-ready GeneSpect™ Somatic Reporter outputs summarize on 1-2 pages variant classifications as well as cancer treatment recommendations. Users build their own local knowledge base with iFlow using in-house clinical findings. Analyses are performed en masse using GeneBucket, a simple tool for parallel analysis of thousands of raw data files, allowing bulk analysis and aggregate data reporting.