Precision Genome Engineering: From Basic Mechanisms to Application

Mar 09–12, 2026 | Fairmont Banff Springs, Banff, AB, Canada
Scientific Organizers: Jonathan S. Weissman, Cecilia Cotta-Ramusino, and Joseph Bondy-Denomy

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Mar 09–12, 2026 | Fairmont Banff Springs, Banff, AB, Canada

Scientific Organizers: Jonathan S. Weissman, Cecilia Cotta-Ramusino, and Joseph Bondy-Denomy

Supported by:

***Meeting program subject to change.

Available Formats:   = In Person     = On Demand
Monday, March 9, 2026
Registration
4:00–8:00 PM
 Van Horne Foyer
Welcome Mixer
6:00–8:00 PM
 Van Horne Foyer
Tuesday, March 10, 2026
Breakfast
7:00–8:00 AM
 President's Hall
Welcome Remarks (Joint)
8:00–8:10 AM
 Van Horne A/B
Keynote Session (Joint)
8:10–9:00 AM
 Van Horne A/B
Jennifer A. Doudna, HHMI/University of California, Berkeley
CRISPR Enzyme Evolution and Applications
Delivery (Joint)
9:00–11:00 AM
 Van Horne A/B
Daniel J. Siegwart, University of Texas Southwestern Medical Center
New LNP Modalities for Target Lung, Heart and Other Tissues
Michael A. Fischbach, Stanford University
Engineered Viral-Like Particle for Targeted Delivery of Gene Editors
Leah R Sabin, Regeneron Pharmaceuticals
Antibody-AAV Targeting: Fundamental Principle Behind Achieving BBB Crossing
Coffee Break
9:30–9:50 AM
 Van Horne Foyer
Award Recipient Acknowledgement
9:50–9:55 AM
 Van Horne A/B
Poster Setup
11:00–1:00 PM
 Van Horne C
On Own for Lunch
11:00–5:00 PM
Poster Viewing
1:00–10:00 PM
 Van Horne C
Symposia Spotlight 1
2:30–4:30 PM
 Van Horne A
Clare Cahir, The Rockefeller University
Cap1 Forms a Cyclic Tetra-adenylate-induced Membrane Pore during the Type III-A CRISPR-Cas Immune Response
Chris J Frangieh, Columbia University Medical Center
Resolving Ambiguity from Variants of Uncertain Significance by Linking Variants, Phenotype, and Allele-specific Expression Bias in Inborn Errors of Immunity
Bria Macklin †, Gladstone Institutes
Mutation Agnostic CRISPR Therapeutics to Treat Dominant Neurodegenerative Disease
Bushra Raj, University of Pennsylvania
High throughput in vivo Mapping of Signaling Histories with CRISPR Barcodes
Shengdar Q Tsai, St. Jude Children's Research Hospital
High-throughput Biochemical and Cellular Approaches towards Developing a CRISPR Therapeutic Genome Editing Platform
Christopher Baehr, UC Berkeley
Chemically Modified CRISPR Enzymes for Multi-organ Genome Editing in vivo
Wayne Ngo, University of California, Berkeley
Amplifying Editing Efficiencies by Making Genome Editing Vesicles in the Body
Wells Burrell, New York Genome Center
Rational Design of Synthetic Proteins Using a Genome-Scale CRISPR Screen
Coffee Available
4:30–5:00 PM
 Van Horne Foyer
New Editing Modality
5:00–7:00 PM
 Van Horne A
Samuel H Sternberg, Columbia University
CRISPR Guided Transposons
Cecilia Cotta-Ramusino, Tessera Therapeutics
Discovery and Application of New Gene Editing Modalities to Treat Disease
Erik J Sontheimer †, University of Massachusetts Medical School
Short Talk: Prime Assembly with Linear DNA Donors Enables Large Genomic Insertions
Social Hour with Dinner
7:00–8:00 PM
 President's Hall
Poster Session 1
7:30–10:00 PM
 Van Horne C
Wednesday, March 11, 2026
Breakfast
7:00–8:00 AM
 President's Hall
Understanding and Therapeutic Application of CRISPR
8:00–11:00 AM
 Van Horne A
Emma Wang, YolTech Therapeutics
Design of Therapeutic Editors Aided by AI and High Throughput Approaches
Xiao Wang, University of Pennsylvania
Developing Bespoke Gene Editing Treatments for Patients with Carbamoyl Phosphate Synthetase 1 (CPS1) Deficiency in Real Time: Successes and Challenges
Britt Adamson, Princeton University
DNA Damage Response and CRISPR
Benjamin P. Kleinstiver, Massachusetts General Hospital
Engineered Technologies for Modifying Single Bases to Several Kilobases
Gerald Schwank, University Zurich
Short Talk: Rescue of Monogenic Obesity by In Vivo Base and Prime Editing in the Brain
Dowoon Gu †, Korea University
Short Talk: Combination of Abasic Substitution and Extension in Guide RNA Inherently Harness Fidelity of SpCas9 for Genome Editing
Coffee Break
9:00–9:20 AM
 Van Horne Foyer
Poster Setup
11:00–1:00 PM
 Van Horne C
On Own for Lunch
11:00–5:00 PM
Poster Viewing
1:00–10:00 PM
 Van Horne C
Career Roundtable (Joint)
3:00–4:30 PM
 Van Horne B
Coffee Available
4:30–5:00 PM
 Van Horne Foyer
Intersection of Gene Editing High Throughput Screening and Machine Learning
5:00–7:00 PM
 Van Horne A
Hyongbum Henry Kim, Yonsei University College of Medicine
Experimental and Machine Learning Approaches to Create New Genome Editing Tools
Jonathan S. Weissman, Whitehead Institute, HHMI, and MIT
In vivo Multiple Modal Information-Rich CRISPR Screens
Randall J. Platt, ETH Zurich
Functional Genomic Approaches
Charles Gersbach, Duke University
Short Talk: Cell Reprogramming by CRISPR-based Activation of Endogenous Master Transcription Factors
Noa Oded Elkayam, EmendoBio
Short Talk: AI-Enhanced Optimization of OMNI Nucleases Expands the CRISPR Toolbox for Therapeutic Applications
Social Hour with Dinner
7:00–8:00 PM
 President's Hall
Poster Session 2
7:30–10:00 PM
 Van Horne C
Thursday, March 12, 2026
Breakfast
7:00–8:00 AM
 President's Hall
Therapeutic Application
8:00–11:00 AM
 Van Horne A
Jennifer Gori, Prime Medicine, Inc.
Application of Prime Editing to Treat Disease
Haihua Chu, Beam Therapeutics
Unlocking the Potential of base Edited HSCs for Therapeutic Applications with Epitope Engineering
Laura Sepp-Lorenzino, Intellia Therapeutics
TTR Therapies
Luigi M Naldini, San Raffaele Telethon Institute for Gene Therapy
Gene Editing: Therapeutics and Genotoxicity
X. Shawn Liu, Columbia University Medical Center
Short Talk: Epigenetic Silencing of Pathological Allele in Inborn Errors Immunity by CRISPR-IMPRINT
Sarah Pierce, Broad Institute
Short Talk: Prime Editing-installed Suppressor tRNAs for Disease-Agnostic Genome Editing
Coffee Break
9:00–9:20 AM
 Van Horne Foyer
On Own for Lunch
11:00–5:00 PM
Symposia Spotlight 2
2:30–4:30 PM
 Van Horne A
Shirley P Chia, National University of Singapore
Variant-By-Variant Activity Profiling Reprograms A CRISPR-Associated Transposon Towards Precise DNA Insertion
Phoebe A Rice, University of Chicago
Structural Basis for Directionality of Large Serine Integrases
Sébastien Levesque, Boston Children's Hospital - Harvard Medical School
In Cellulo DNA Assembly for Targeted Genomic Integration and Rearrangement in Human Cells
Shannon M Miller, Scripps Research
Programmable CRISPR-free gene insertion
Holt A Sakai, Broad Institute
Directed Evolution of Small RNA-stabilizing Motifs that Improve Prime Editing
Lilly van de Venn, ETH Zurich
AutoDISCO Enables Sensitive and High-throughput CRISPR/Cas Off-target Detection in Cells and Organisms
Kah Min Yap, Peter MacCallum Cancer Centre
Rewiring Endogenous Genes in CAR T Cells for Tumour-Restricted Payload Delivery
Aditya V Ansodaria, UMass Chan Medical School
Enhancing the Efficacy and Purity of Prime Editing using Chemically Modified Editing Templates and Modification-Tolerant Polymerases
Coffee Available
4:30–5:00 PM
 Van Horne Foyer
CRISPR Biology
5:00–6:45 PM
 Van Horne A
Joseph Bondy-Denomy, University of California, San Francisco
AntiCRISPR Phage Defense Against CRISPR Systems
Mitchell R. O'Connell, University of Rochester Medical Center
Pulling the Plug on Bacteriophage Infection: The Pore Behavior of CRISPR and Anti-phage Defense Associated Membrane Proteins
Elizabeth Kellogg, St. Jude Children's Research Hospital
Mechanism of Programmable Transposases
Kazuo Nakamura, Gladstone Institutes
Short Talk: Phage Defense and Genome Editing using Novel Retrons Sourced from Isolated Environmental Bacteria
Meeting Wrap-Up: Outcomes and Future Directions
6:45–7:00 PM
 Van Horne A
Social Hour with Dinner
7:00–8:00 PM
 President's Hall
Cash Bar
8:00–11:00 PM
Entertainment
8:00–11:00 PM
Friday, March 13, 2026
Departure
12:00–11:59 PM

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