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2026 Keynote Speakers

Kathleen Burns headshot.png

Our group was among the first to develop methods for comprehensively mapping mobile DNA insertion sites in the human genome, which underscored that these are a significant source of structural variation (Cell, 2010). We have since studied the functional effects of inherited mobile element insertions using a combination of genetic approaches and molecular biology (Proceedings of the National Academy of Sciences, 2017) and are exploring their contributions to somatic mosaicism across human tissues. Our group has also shown that the expression of long interspersed element-1 (LINE-1, L1) ORF1p is a hallmark of human cancers (American Journal of Pathology, 2014), and that somatically-acquired L1 insertions occur during cancer evolution (Nature Medicine, 2015). Our lab is currently studying consequences of this activity for DNA repair and chromosomal instability in cancer cells (Nature Structural and Molecular Biology, 2020bioRxiv) and seeking to translate our understanding of this basic biology to improve our approaches to cancer diagnostics and therapeutics.

Siyuan Wang headshot_edited.jpg

Wang’s independent lab at Yale is devoted to understand mammalian genome architectures and spatial transcriptome in health and disease. In the past few years, the lab introduced a new integrative technique, termed Multiplexed Imaging of Nucleome Architectures (MINA) – the first comprehensive 3D nucleomic imaging technique (bioRxiv 2019Nat Comm 2020Nat Protoc 2021). This method enabled multi-omic and multiscale visualization of single-cell nucleome architectures and gene expression to functionally define promoter-enhancer interactions, chromatin domains, compartments, territories, and chromatin interactions with nuclear landmarks in the same single cells of complex mammalian tissues, generating true 3D maps of all major chromatin architectures reported by various sequencing methods (P-E loops, TADs, LADs, NADs, A-B compartments, and chromosome territories). In applying the technique to mouse fetal liver, the team discovered cell-type-specific chromatin architectures associated with gene expression as well as chromatin organization principles independent of cell type (bioRxiv 2019Nat Comm 2020). They also applied chromatin tracing to elucidate novel architectures and their regulation in the folding conformations of the two copies of X chromosomes in female human cells (Genome Biology 2021; Science Advances 2023). Overall, the chromatin tracing and MINA technologies have revolutionized 3D genomics and multi-omics studies (Trends in Cell Biology “Best of 2021”Nature Reviews Methods Primers 2024).

Hovestadt Headshot.png

I am a computational biologist at Dana-Farber/Boston Children's Cancer and Blood Disorder Center and Assistant Professor of Pediatrics at Harvard Medical School. My lab and I study pediatric brain tumors, the leading cause of cancer-related death in children. Treating children with brain tumors remains a major challenge as effective therapies are often lacking. We develop and apply novel genomic and computational tools to better understand cancer biology, diagnose tumors more accurately, and treat patients more effectively.

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