Cell‐Free DNA Sequencing for Early Cancer Detection
Learning Objective #1 Understand some of the challenges with the collection, generation, and interpretation of liquid biopsy data in clinical studies Learning Objective #2 Become acquainted with different biological aspects of cell-free DNA and associated technologies to detect early cancer Learning Objective #3 Become acquainted with initatives in hereditary cancer to assess the use of cell-free DNA sequencing technologies for cancer screening Our speaker will give an overview of the technology, utilization and challenges of liquid biopsy, which is a newer testing methodology that the general genetic counseling community may not have significant knowledge of. Dr. Trevor Pugh, PhD, FACMG is a cancer genomics researcher, board-certified molecular geneticist, and holder of the Canada Research Chair in Translational Genomics. He is Director of the Joint Genomics Program of the University Health Network and Ontario Institute for Cancer Research which supports basic, translational, and clinical research. He is appointed as an Associate Professor in the University of Toronto Department of Medical Biophysics, Senior Scientist at the Princess Margaret Cancer Centre, and Senior Investigator at the Ontario Institute for Cancer Research. His research lab is focused on understanding clinical implications of clonal shifts in cancer and immune cells during treatment, most recently using cell-free DNA, immune repertoire, and single cell RNA-seq sequencing. Most recently, he was recognized by Canada's Top 40 Under 40, a Terry Fox New Investigator Award, and inclusion on the Web of Science Highly Cited Researchers List.

"Circulating tumour DNA: An increasingly powerful diagnostic tool for oncology" - Nitzan Rosenfeld

How to Read a Cancer Genome | Part 1: The basics of cancer genomics

Next-generation sequencing in MPNs: unlocking diagnostic precision and prognostic power

Genome vs Exome sequencing; everything you should know

Next Generation Sequencing 1: Overview - Eric Chow (UCSF)

Fatty Acid Balance - Mind the Gap: Re-examining the Evidence in Preterm Lipid Emulsions

BioSkryb Seminar: A Revolution in Single Cell Genomics featuring ResolveDNA™ and ResolveOME

RMIE 2022: Updates in Colon Cancer Screening

How to Read a Cancer Genome | Webinar 2: Tertiary analysis beyond driver mutations

Bioinformatic Approach for Drug Discovery FKUH

Individualized Neoantigen‑Targeted Vaccines for Lung Cancer #tijc

Imaging Flow Cytometry: A Brief Overview - Andrew Filby (Newcastle U.)

Rocky Mountain Highlights 2023 I Session I: High Yield Topics in Luminal Gastroenterology

Sequencing, Variant Calling, and Cancer Genomics

ctDNA and MRD | 2023 Best of GI Cancer Conference

View Point Toronto 2025 - Stem Cells & Regenerative Therapies for Retinal Disease

Brian Evavold - "Catch bond engineering of the T cell receptor"

Next-Generation Sequencing Technologies - Elaine Mardis (2014)

DNA graffiti: mutation patterns in cancer | The Royal Society

