We are looking forward to seeing you in Houston to discuss exiting new Genomic Solutions for your research.
Put Booth #1021 on your list for inspiration!
BGI offers a complete line of NGS services, and the world’s broadest portfolio of Whole Genome Sequencing services including True PCR-free WGS, low-pass WGS, with prices starting from an amazing $600. We will announce new clinical-grade WGS solutions as well as a new long-read WGS service, all from our unique DNBseq™ sequencing technology.
We support your academic research or pharmaceutical R&D projects: From single sample to large-scale population studies, we are at your service!
At our lunch seminar
NGS 2.0 – Innovation results in new value to Genomic Research and Clinical utility.
You will learn how a novel barcoding strategy offers long read benefits for advanced genomic applications and how new sequencing technology offers new diagnostic options.
Thursday, October 17, 12:45 – 2:00PM
Hilton Americas-Houston, Lanier Ballroom CF, Level 4
Box lunch will be provided
Talks and Speakers:
Towards a perfect genome with long single-molecule sequencing technology: New opportunities for advanced genomic applications
Brock Peters, Ph.D.
Sr. Director, Research, Complete Genomics/ MGI
Clinical NGS: Exome vs Genome Sequencing
Xia Wang, Ph.D., FACMG
Co-Founder & Chief Diagnostic Officer AiLife Diagnostics
NEW SERVICE PRODUCTS
We will present exciting new services, including new synthetic long-read services to help you advance your genomic research, and clinical-grade Whole Genome Sequencing to help putting Genomics to work in healthcare applications.
(Check back with us in the coming months as we develop more content leading up to ASHG)