See how the GeneReader NGS System can bring NGS to your lab in just 30 days
Fragmented workflows, the requirement for bioinformatics expertise to achieve meaningful insights from data, and prohibitive initial set up costs, can make adoption of next-generation sequencing (NGS) technology challenging for smaller labs. Let our two NGS experts guide you through the process of implementing NGS in your lab using a complete integrated NGS system. Our webinar will walk you through all steps of the NGS workflow including data analysis and interpretation. Our experts will also share their experiences and data generated by early adopters of the GeneReader NGS system from around the globe.
Title: NGS live in your lab in 30 days
Speakers: Dr. Yi Kong and Salim Essakali
Title: NGS live in your lab in 30 days
Speakers: Dr. Yi Kong and Salim Essakali
NGS in 30 days made possible by the unique design of the GeneReader NGS System:
- The world’s first truly complete NGS workflow: All components of the workflow, from sample prep to sequencing and data interpretation, designed together to work in synchronization.
- Actionable Insights: Designed with the central goal of generating a simple, clear report of only the most relevant variants.
- Flexible to fit your current and future needs: Design elements and automation solutions to match the throughput needs of your lab.
- Guaranteed results with predictable costs: A single NGS provider means complete pricing transparency from sample to result.
- Proven expertise and service: Our team of NGS specialists are ready to support you in efficiently implementing, validating and operating the GeneReader in your lab.