Ph.D., Chief Genomics Officer, Broad Inst.
Biography
Stacey Gabriel is a human geneticist with a research interest in large-scale genomics research. The organization that she leads operates as one of the largest sequencing centers in the world and continually explores, validates, optimizes, and implements new technologies, methods, and analysis tools to meet the needs of the scientific community. She has played a central role in the development of methods for generating and analyzing data using genomic technologies for both cancer and medical genetics studies. Her research on the haplotype structure of the human genome provided foundation for the Human HapMap Project. She directs the Broad Institute’s execution in flagship large-scale projects including the Human HapMap, the 1000 Genomes Project, The Cancer Genome Atlas, and the All of Us Research Program. During the covid-19 pandemic Dr. Gabriel led the development and execution of a commercial-scale diagnostic testing and viral surveillance activity.
Session Abstract – PMWC 2023 Silicon Valley
Track 4 - January 25 9.00 A.M.-4.45 P.M.
Track Chair: Cindy Lawley, Olink
- How New Public-Private Collaboratives Can Catalyze Transformative Health Breakthroughs
Chair: Keith Yamamoto, UCSF
- Douglas Friedman, Engineering Biology Research Consortium (EBRC)
- Jay Keasling, JBEI (Joint BioEnergy Institute)
- Renee Wegrzyn, ARPA-H - Moving Sequencing into the Clinical Setting
Chair: Charles Chiu, UCSF
- Charlotte Hobbs, Rady Children’s Hospital
- Euan Ashley, Stanford University
- Sivan Bercovici, Karius
- Heike Sichtig, Foundation Medicine - Evolving Sequencing Applications: Spatial Single-Cell Multi-Omics
Chair: Michael Rhodes, NanoString
- Chrstina Curtis, Stanford - How will Cheap Genome Sequencing Impact Genomic Medicine (PANEL)
Chair: Euan Ashley, Stanford
- Shawn Levy, Element Biosciences
- Aleks Rajkovic, UCSF
- David Bentley, Illumina
- Stacey Gabriel, Broad Inst.
- Sean Hofherr, Fabric Genomics - Single-cell, Spatial, and in Situ Technologies
Chair: Dina Finan, 10x Genomics
- Carina Emery, Miltenyi Biotec - Combining WGS with a AI-based Tumor Enrichment Method
Chair: Asaf Zviran, C2I
- Multi-omics Approaches Supporting Clinical Translation
Chair: Cindy Lawley, Olink
- Erin Smith, Takeda
- Si Wu, Stanford
- Christopher Whelan, J&J - Molecular Diagnosis New standard with NGS for Neurological and Infectious Conditions
Chair: Scott Rabuka, DNA Genotek
- Forrest Wright, Quadrant Laboratories
- Frank Middleton, SUNY Upstate Medical University - PMWC Showcase
- Josh Lauer, Ultime
- Olivier Lucas, Oxford Nanopore
- Lukasz Boryn, Ardigen
