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ASHG – Booth #748
10월 17, 2017 - 10월 21, 2017
The Annual Meeting of the American Society of Human Genetics (ASHG) is the largest human genetics meeting and exposition in the world. This year’s meeting is expected to attract over 6,500 scientific attendees, plus almost 250 exhibiting companies. The meeting provides a forum for the presentation and discussion of cutting-edge science in all areas of human genetics. We are looking forward to meeting you at any of our 10x Genomics events!
10x Community Mixer
Join us at the Hyatt Regency Express Terrace in Orlando, FL to kick off ASHG 2017 at the 10x Community Mixer! Space is limited, so register today to reserve your spot at this fun-filled evening complete with drinks, appetizers, and good company!
Tuesday, October 17, 2017
7:00 PM – 11:30 PM
Hyatt Regency, Regency Express Terrace
Advancing Genomic and Single-Cell Sequencing Drop-by-Drop with the 10x Chromium System
To truly understand disease mechanisms, heritability, potential diagnoses and development of therapies, we need higher resolution and more complete genomic information. With the Chromium System from 10x Genomics, the ability to resolve ambiguous single nucleotide variants, determine phasing and haplotype information, and identify complex structural variants is at your fingertips. Whether you want to overcome the limitations of current short-read technology to obtain long-range information with Linked-Reads or dissect cell-type differences by profiling hundreds of thousands of cells, our solutions empower you to accelerate the pace of discovery. Lunch will be provided, so reserve your spot today!
Wednesday, October 18, 2017
12:30 PM – 1:45 PM
Hyatt Regency, Regency U, Convention Level
Intuitive Tools for Sequence Analysis: Crunching Genomic, Single-Cell, and Immune Repertoire Data Using 10x Chromium Software
Our software and visualization tools are designed to take the guesswork out of analyzing and visualizing genome, single-cell, and immune repertoire data. In this interactive workshop, you will learn:
- How to harness the power of Linked-Reads for your genome and de novo applications with Long Ranger and Supernova Software.
- How to elegantly visualize your genome data with our Loupe Genome Browser.
- How the Loupe Browser and Loupe V(D)J Browser can be used to quickly and interactively identify cell types or explore the diversity of T-cell receptors at the single-cell level.
Breakfast will be provided, so reserve your spot today!
Thursday, October 19, 2017
7:15 AM – 8:45 AM
Hyatt Regency, Celebration 3/4, Convention Level