The human genome is made of about 3 billion base pairs of DNA — but much of it remains a mystery. Scientists understand the 2% of the human genome that codes for proteins relatively well, but have only limited knowledge of the remaining 98%. Our AlphaGenome model has already shown how single changes in these non-coding DNA regions can disrupt molecular processes like protein production, but the bigger picture remained unclear.
Today, we're introducing AlphaGenome Atlas, a database that predicts the effects of every possible single nucleotide variant in the human genome. We used the AlphaGenome AI model to pre-calculate the regulatory impact of all 9 billion single-letter genetic changes, resulting in a massive, 1-petabyte dataset. Our new Atlas helps scientists rapidly query this vast information.
To help researchers rapidly navigate this, the Atlas introduces the AlphaGenome Variant Impact (AVI) score. This single, easy-to-use score combines predictions for both coding and non-coding regions, allowing researchers to quickly prioritize the most promising avenues for research without sifting through thousands of data points.
AlphaGenome Atlas is already acting as a powerful augmentation partner for the scientific community, accelerating research in areas like:
AlphaGenome Atlas is available today through an intuitive website portal that requires zero coding skills, democratizing access for clinical researchers and biologists worldwide. This is part of our ongoing commitment to accelerate genomic discovery and science, for everyone.
AlphaGenome Atlas provides grounded genomic insights that will accelerate the pace of biological discovery.
Read more on the Google DeepMind blog.