
Explore AlphaFold's revolutionary impact on protein structure determination with Dame Janet Thornton. Discover how this AI program is transforming bioinformatics and its potential future applications.

Explore Harmonic Persistent Homology for analyzing multi-omics data, uncovering hidden patterns in complex diseases, and identifying biomarkers associated with latent biological pathways.

Explore machine learning approaches for analyzing large-scale time series and spatio-temporal data, with applications in healthcare and climate modeling.

Explore Python's ecosystem for single-cell data analysis with scverse, a community-driven initiative coordinating omics data work.

Explore fundamental computational methods in physics and chemistry, presented by their creators, with insights into their development and applications.

Explore cutting-edge single-cell genomics research, featuring expert talks on spatial transcriptomics, multi-omics, and bioinformatics from leading institutions in Atlanta and across America.

Comprehensive exploration of single-cell RNA sequencing, covering technologies, applications, and analysis techniques. Discusses advantages over bulk sequencing and addresses key biological questions in the field.

Comprehensive overview of computational biology, exploring GenAI, representation learning, and their applications in genomics and language models. Insights into future directions and potential impacts.

Explore computational approaches for quantifying microbial growth determinants, focusing on genotype-environment interactions and their implications for pathogen control and biotechnology.

Explore gene regulatory network rewiring patterns through innovative experimental methods and computational approaches for characterizing effects of perturbations at single-cell level.

Explore promoter and isoform diversity in cancer transcriptomes using long-read RNA sequencing. Gain insights into alternative promoters' role in gene regulation and their impact on cancer research.

Explore a new method for estimating genetic variant effects on transcription factor regulatory events, integrating diverse omics data to build interpretable regulatory networks for disease insights.