Join us for the relaunch of the Genomics Theme! This first webinar is in collaboration with our Statistical Methods for Health Equity Series.

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Topic: 

Bridging Genomics’ Greatest Challenge: The Diversity Gap

Abstract:

Drawing on recent findings from genome-wide association studies, pharmacogenomics, clinical trials and directo to consumer genetics, this talk highlights the critical role that diverse reference panels play in enabling precise diagnoses, treatments, and risk assessments. It illustrates how current biases—whether geographic, ancestral, or sex-based—undercut health outcomes for large segments of the world population, and explains how inclusive data collection can help mitigate these inequities. By showcasing cases such as heightened adverse drug reactions in underrepresented groups, the discussion provides evidence for why genome research must pivot from a one-size-fits-all paradigm toward equitable, data-driven solutions. Ultimately, this talk underscores the right to science for all, advocating for a future in which the benefits of genomics research are universally accessible and yield tangible improvements in global health.

Speaker bio:

Dr Manuel Corpas is an internationally recognised leader in genomics, bioinformatics, and health data science. As President of the Spanish Congress of Genomic Medicine, he has expanded access to precision medicine in Spanish-speaking communities, particularly among underrepresented populations in Latin America. His pioneering work in population genomics—including large-scale sequencing initiatives such as the Peruvian Genome Project—has shed light on genetic diversity and health disparities. A driving force behind tools like BioJavaScript and the DECIPHER database, Dr Corpas has advanced big data initiatives and rare disease diagnostics. His advocacy for open science is reflected in contributions to global efforts such as ELIXIR, GOBLET, and Deciphering Developmental Disorders. He has also set new standards in data governance through principles of equity, diversity, and inclusion from the Global Alliance for Genomics and Health. With over 80 peer-reviewed publications, fellowships from the Alan Turing Institute and the Software Sustainability Institute, and an unwavering commitment to inclusive genomic medicine, Dr Corpas continues to bridge the gap between raw data and tangible healthcare improvements for all.

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Please direct any questions about the webinar series to info.dsxhe@gmail.com