This current project is effectively a cache database for an earlier tool. The earlier project is where the main impact is - predicting the functional effect of a variant in the human genome.
For this updated project, they effectively ran the earlier tool for all possible variants in the genome (3 billion bases in the genome * 3 single nucleotide variants = 9 billion). It’s a very useful project for people like me, but the major advance was already done (admittedly by the DeepMind team).
For this updated project, they effectively ran the earlier tool for all possible variants in the genome (3 billion bases in the genome * 3 single nucleotide variants = 9 billion). It’s a very useful project for people like me, but the major advance was already done (admittedly by the DeepMind team).