--(BUSINESS WIRE)--10X Genomics:
“Upgrade Your Sequencing Data with Structural Variants and Haplotype Phasing”
| WHEN: | Thursday, October 8, 2015, 1 – 2:30 p.m. ET | |||
| WHERE: | Sheraton Inner Harbor Hotel | |||
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Severn Room, 2nd Floor |
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| 300 S Charles St | ||||
| Baltimore, MD 21201 | ||||
| WHO: | Featured speakers: | |||
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• Hanlee Ji, Stanford University |
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• Serafim Batzoglou, Stanford University |
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• Michael Schnall-Levin, 10X Genomics |
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| WHAT: | "Upgrade Your Sequencing Data with Structural Variants and Haplotype Phasing" | |||
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10X Genomics will host a workshop to describe the GemCode™ System and highlight data generated using the platform. Leading industry experts will discuss deriving insights based on uncovering massive numbers of new single nucleotide variants in critical genomic regions, detecting novel structural variations, and showcasing information provided by haplotype phasing. |
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Attend the workshop to learn more about upgrading your short-read sequence data to unlock novel sequence variant information. Attendees are also encouraged to visit the 10X Genomics booth #216. |
ABOUT 10X GENOMICS
10X Genomics is changing the definition of sequencing™ by providing an innovative genomics platform that dramatically upgrades the capabilities of existing short read sequencers. The Company does this through a combination of elegant microfluidics, chemistry and bioinformatics. With the GemCode Platform, researchers can now find structural variants, haplotypes, and other valuable long range information while leveraging existing sequencing workflows.
Chempetitive Group for 10X Genomics
Trisha Rule, 858-230-4949
trule@chempetitive.com
