2022 Agenda
Thursday, September 8, 2022 (Evening)
5:05 p.m. – 5:10 p.m.
Welcome
Session I: New Technologies and Broad Perspectives in Genomic Medicine (Eric Green, National Human Genome Research Institute and Michael Talkowski, Massachusetts General Hospital and Broad Institute Chairs)
5:10 p.m. – 5:45 p.m.
Karen Miga
University of California, Santa Cruz
5:45 p.m. – 6:20 p.m.
Diana Bianchi
National Institute of Child Health and Human Development (NICHD) and National Human Genome Research Institute (NHGRI)
6:20 p.m. – 6:55 p.m.
Daniel MacArthur
Center for Population Genomics, Garvan Institute of Medical Research
6:55 p.m. – 7:15 p.m.
Emily Mrig (Abstract Selected)
University of California San Francisco
“When covering and discovering are at odds: How the logic of health insurance undercuts the promise of precision medicine for people with hereditary cancer risks”
7:15 p.m. – 10:00 p.m.
Welcome Reception
Friday, September 9, 2022 (Morning)
7:30 am – 9:00 am
Breakfast
Session II: Genomic Medicine I: Prenatal Diagnostics (Wendy Chung, Columbia University and Diana Bianchi, NICHD, Chairs)
9:00 a.m. – 9:25 a.m.
Ronald Wapner
Columbia University Irving Medical Center
9:25 a.m. – 9:50 a.m.
Hamish Scott
University of South Australia, Centre for Cancer Biology
9:50 a.m. – 10:15 a.m.
Gretchen Bandoli
University of California, San Diego
10:15 a.m. – 10:35 a.m.
Harrison Brand (Abstract Selected)
Massachusetts General Hospital
“A comprehensive and non-invasive fetal screen of all coding variation”
10:35 a.m. – 11:05 a.m.
Coffee Break/Exhibit Hall
Session III: Panel Session: Economic Barriers and Predictive Value to Genome Sequencing in Precision Medicine (Kathryn Phillips, University of California San Francisco, Chair)
11:05 a.m. – 12 p.m.
Phil Febbo
Illumina
Keith Yamamoto
UCSF
Sharon Terry
Genetic Alliance
Friday, September 9, 2022 (Afternoon)
12:00 p.m. – 1:10 p.m.
AGBT Lunch
1:15 p.m. – 1:40 p.m.
Sponsor Workshops
Diamond Sponsor- DNA Script
1:40 p.m. – 2:00 p.m.
Sponsor Workshops
Emerald Sponsor- FABRIC Genomics
Session IV: Genomic Medicine II-Rare Disease and Global Initiatives (Heidi Rehm, Massachusetts General Hospital and Broad Institute and Professor Dame Sue Hill, NHS England, Chairs)
2:00 p.m. – 2:30 p.m.
Euan Ashley
Stanford University
2:30 p.m. – 3:00 p.m.
Sharon Terry
Genetic Alliance
3:00 p.m. – 3:20 p.m.
Bruce Korf (Abstract Selected)
University of Alabama Birmingham
“The Alabama Genomic Health Initiative: Five years In”
3:20 p.m.- 5:20 p.m.
Poster Session & Exhibit Hall, Wine and Cheese Reception
6:30 p.m. – 9:00 p.m.
AGBT dinner
Saturday, September 10, 2022 (Morning)
7:30 a.m. – 9:00 a.m.
Breakfast
Session V: Advances in Genome Biology (Howard McLeod, Precision Health, Intermountain Healthcare and Len Pennacchio, Lawrence Berkeley National Laboratory, DOE Joint Genome Institute, Chairs)
9:00 a.m. – 9:30 a.m.
Kelly Frazer
University of California San Diego
9:30 a.m. – 10:00 a.m.
Stephen Montgomery
Stanford University
10:00 a.m. – 10:20 a.m.
Caralynn Wilczewski (Abstract Selected)
National Human Genome Research Institute
“Genotype first: Clinical genomics research through a reverse phenotyping approach”
10:20 a.m. – 10:55 a.m.
Coffee Break & Exhibit Hall
11:00 a.m. – 12:00 p.m.
Fireside Chat: Patient stories (Stephen Kingsmore, Rady Children’s Hospital, Chair)
Nathaly Sweeney
Assistant Professor of Pediatrics, Neonatal-Perinatal Medicine, University of San Diego, and Rady Children’s Hospital
Jerica Lenberg
Genetic Counselor and Rady Children’s Institute for Genomic Medicine
The Wingate Family
12:00 p.m. – 1:00 p.m.
AGBT Lunch
1:00 p.m. – 1:15 p.m.
Sponsor workshop
Sapphire Sponsor-Cambridge Consultants
1:15 p.m. – 1:27 p.m.
Sponsor workshop
Ruby Sponsor-Beckman Coulter Life Sciences
Session VI: National Initiatives in Genomic Medicine: All of Us and Genomics England (Geoffrey Ginsburg, All of Us Research Program, NIH and Professor Dame Sue Hill, NHS England, Chairs)
1:30 p.m. – 1:40 p.m.
Overviews from the Chairs
–
1:40 p.m. – 1:55 p.m.
1:55 p.m. – 2:15 p.m.
2:15 p.m. – 2:35 p.m.
The All of Us Research Program
Anji Musick, All of Us Research Program
“Data Resources and Programs”
Eric Venner, Baylor College of Medicine
“Emerging Results”
Niall Lennon, Broad Institute of MIT and Harvard
“Taking the long view: driving discovery and advancing genomic medicine with new data types in AoU”
–
2:35 p.m. – 3:00 p.m.
3:00 p.m. – 3:25 p.m.
Genomics England
Richard Scott, Chief Medical Officer, Genomics England
Augusto Rendon, Chief Bioinformatician, Genomics England
3:25 p.m. – 3:45 p.m.
Coffee Break
Session VII: Neurodevelopmental Genomics (Penelope Bonnen, Baylor University and Kaitlin Samocha, Massachusetts General Hospital, Chairs)
3:45 p.m. – 4:15 p.m.
Stephan Sanders
University of California, San Francisco
4:15 p.m. – 4:45 p.m.
Kaitlin Samocha
Massachusetts General Hospital
4:45 p.m. – 5:15 p.m.
Allyson Berent
FAST
5:15 p.m. – 5:20 p.m.
