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Topics Covered
- Computational genomics
- Structural variants
- Tandem repeats
- Long-read sequencing
- Genomic variant calling
- Epigenetics and methylation
- AI and machine learning in genomics
- HLA genomics
- LPA and cardiovascular disease
- Academic-industry collaboration
Biography
Dr. Fritz Sedlazeck is an Associate Professor at the Human Genome Sequencing Center at Baylor College of Medicine and an Adjunct Associate Professor at Rice University. His research focuses on algorithmic developments and high-performance computing for genomic and genetic applications. Specifically, he studies ways to improve the characterization of complex genomic alterations between individuals’ genomes based on large genomic sequencing data and as such improve our understanding of complex phenotypes such as human diseases.
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Talk Citation
Sedlazeck, F. (2026, October 29). Optimising collaboration between lead identifiers and genomic analysts in pharma and biotech companies [Audio file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved October 29, 2026, from https://doi.org/10.69645/XQJB5671.Export Citation (RIS)
Publication History
- Published on October 29, 2026
Financial Disclosures
- Dr. Fritz Sedlazeck has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Audio Interview
Optimising collaboration between lead identifiers and genomic analysts in pharma and biotech companies
Published on October 29, 2026
20 min