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Ultima Genomics
Join us at ASHG!

Come see how our customers are unleashing a new era in high-throughput genomics

ASHG 2023 | Washington, D.C. | November 1st - 5th

Be sure to attend our Industry Education Session in Room 140AB, and visit us in Booth 1823 as leaders in genomics show how they are deploying a variety of applications on the Ultima platform, taking advantage of the lowest-cost, highest-throughput sequencing architecture.


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INDUSTRY EDUCATION SESSION

Thursday, November 2 | Conference Center, Room 140AB, Level 1 | Talks 3:30 PM - 4:30PM

Empowering Genomics at Scale

Join us for talks highlighting the role of deep learning in genomics and some of the exciting research and data being generated on Ultima Genomics’ new sequencing platform. Learn how the 100 UG™ sequencer is empowering scientists to conduct genomics studies at unprecedented scale and cost.

Introduction

Gilad Almogy, Ph.D., Chief Executive Officer, Ultima Genomics


Acceleration of Deep Learning for Data Processing in Genomics

George Vacek, Global Head of Genomics Alliances, NVIDIA


A high-throughput, automated ATAC-seq reveals quantitative regulatory effects of transcription factor dosage

Betty Liu, Stanford University (Greenleaf Lab)


Comprehensive variant analysis in clinical samples by cost effective whole genome sequencing

Doron Lipson, Ph.D., Chief Scientific Officer, Ultima Genomics

The updated standard reference Genome-in-a-Bottle (GIAB) data set presented will be published immediately after the talk



TALKS

Thursday, November 2 | Convention Center, Ballroom A, Level 3 | 9:30 - 9:45AM

Clinical utility of deep-RNAseq in Mendelian disorder diagnostics

Sen Zhao, Baylor College of Medicine



POSTERS

Thursday, November 2 | 3:00 – 5:00pm

PB3183 | Comprehensive variant analysis in clinical

samples by cost effective whole genome sequencing

Sarah Pollack, Ultima Genomics



Friday, November 3 | 3:00 – 5:00pm

PB3305 | A high-throughput, automated ATAC-seq reveals quantitative regulatory effects of transcription factor dosage

Betty Liu, Stanford (Greenleaf Lab)

PB3389 | Germline short variants detection from UG100 Sequencing Data

Doron Shem-Tov, Ultima Genomics



Saturday, November 4 | 2:15 – 4:15pm

PB3363 | Detection of germline copy number variation from whole genome sequencing on UG100: A cost-effective and robust approach

Tammy Biniashvilli, Ultima Genomics

PB3351 | Cost-effective, high-resolution whole transcriptome sequencing for gene fusion detection applications

Jennifer Pavlica, Watchmaker Genomics

MEET US

Interested to learn more about Ultima Genomics?

We will be meeting partners throughout the conference to discuss their high-throughput applications.

Email events@ultimagenomics.com to request a meeting.

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