Resources & Education

GGMC Educational Webinar Series

Upcoming Webinar:
January 30th. 7am PT–10am ET / 4pm GMT+2

Join Us Each Month

The GGMC Educational Webinar Series brings together leaders, educators, researchers, and professionals with all levels of expertise to share health sciences initiatives taking place in their respective fields and countries.

Each month’s webinar will feature new guest speakers offering novel insights into their fields. The virtual platform allows us to reach a global audience, particularly those in low-and middle income countries (LMICs) where our organization’s mission is heavily focused. This monthly series is free and open to anyone who wishes to participate.

Join us as we come together each month to share scientific ideas, best practices, challenges, lessons learned, funding opportunities, and more as we continue our mission of improving population health for all.

Upcoming Webinar

"The GA4GH Phenopacket Schema, A Computable Representation of Clinical Data."

January 30th. 7am (PT) – 10am (ET) / 4pm (GMT +2)

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Dr. Mónica Muñoz Torres

Dr. Mónica Muñoz Torres is an Associate Professor of Biomedical Informatics at the University of Colorado Anschutz Medical Campus. She has dedicated her career to developing software tools and standards for analyzing and disseminating data resources in the biological sciences. Her expertise spans genomics, biocuration, knowledge representation, data harmonization, and artificial intelligence. Her research is motivated by her passion for leveraging comparative genomics to advance our understanding of human health and disease. Through translational, integrative, and semantic data
science, she aims to improve socio-technological practices, build research communities, and increase diversity in the genomics and bioinformatics fields.

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Dr. Peter N. Robinson

Peter Robinson, Professor and Donald A. Roux Chair, Genomics and Computational Biology, leads a research group dedicated to the development of algorithms and computational resources for genomics. Peter is a PI of the Monarch Initiative, an NIH supported project dedicated to the integration, alignment, and re-distribution of cross-species gene, genotype, variant, disease, and phenotype data. Highlights of the lab’s work include the Human Phenotype Ontology, the Exomiser  suite of tools for exome and genome analysis, and algorithms for ChIP-seq and immunogenomics.

Peter studied Mathematics at Columbia College, Medicine at the University of Pennsylvania, and Computer Science at Columbia University. He completed an internship in Primary Care Internal Medicine at Yale University, and a residency (Facharzt) in Pediatrics and obtained a Habilitation (roughly equivalent to a PhD) in Human Genetics at the Charité – Universitätsmedizin Berlin. He led the Bioinformatics group at the Institute for Medical Genetics and Human Genetics at the Charité from 2004-2016. From 2016-2023, he led a research group at the Jackson Laboratory (JAX) for Genomic Medicine in Connecticut, USA. From 2024, his primary affiliation will be with the Berlin Institute of Health (BIH) and he will continue to be affiliated with JAX.

About the Talk

A Phenopacket is a standardized way of sharing disease and phenotype information — that is, a
computer schema to exchange information about a patient’s medical history, including phenotypic
features (physical characteristics, symptoms, and signs of a disease), genetic information (genomic data
linked to the patient), medical conditions, and medical treatments the patient has received. Phenopackets are critical to research on human health because they advance interoperability (phenopackets use ontologies to ensure data from different sources can be easily understood and integrated), data sharing (facilitating the sharing of patient data between researchers, clinicians, and other healthcare providers), machine learning (phenopackets can be used to train machine learning models to improve diagnosis and treatment), and precision medicine (by combining phenotypic and
genetic information, Phenopackets can help identify personalized treatment options for patients).
Phenopackets are a powerful tool for advancing medical research, improving patient care, and accelerating the development of new treatments.

Apply To Be a Speaker

Interested in speaking at an upcoming webinar? Use the form below to provide us with some information on your proposed topic and your availability to speak. 

Previous Webinars (2024)

Presented by Dr. Vindya Subasinghe

Presented by Dr. Lyndon J. Mitnaul

Presented by Dr. Brian J. Carney

Presented by Kawmadi Gunawardena

May 28, 2024: “Integrating Genetics into Tanzanian Healthcare: An Overview”

Presented by Dr. Mohamed Zahir Alimohamed

March 28, 2024: “The All of Us Research Program”

Presented by Dr. Geoffrey S. Ginsburg

February 29, 2024: “A Case for Extracellular Vesicles”

Presented by Prof. Carlos Salomon Gallo

February 15, 2024: “Personalized Therapeutics: Clinical Reality and Future Challenges”

Presented by Prof. George P. Patrinos

Previous Webinars (2023)

December 21, 2023: “Personalized Risk Assessment for Early Detection of Cancer”

Presented by Prof. Nora Pashayan

October 30, 2023: “Challenges, Insights and Outcomes of RDNow”

Presented by Dr. Michelle de Silva

July 27, 2023: “Reflections of a Biomedical Scientist on Four Continents.”

Presented by Dr. Juergen Reichardt

June 27, 2023: “Utility of Broad Scale Proteomics in Population Cohort Studies”

Presented by Dr. Cindy Lawley

February 22, 2023: “Transforming Health in Singapore Through Precision Medicine”

Presented by Prof. Patrick Tan

Older Webinars

2022 WEBINARS

2021 WEBINARS

G2MC Grand Rounds

This series of lectures conducted by G2MC in 2016 showcases some of the primary initiatives in genomic medicine from around the globe during this time, and is a precursor to the journey of G2MC.

We Want to Hear From You!

For questions or feedback regarding the GGMC Educational Webinar Series, or to suggest a speaker for a future meeting, please contact us.