Catalog all genetic and multi-omic variation from genomes sequenced in HGP2;Clarify the clinical relevance of all genetic and multi-omic variation cataloged, and;Embed genomic and multi-omic findings into standard clinical practice and precision public health.
Define clinically actionable reporting and intervention best practices for carrier screening, incidental findings, dominant disorders, rare disease diagnosis, and pharmacogenomics;Implement clinically actionable reporting and intervention for all genomes sequenced within the scope of HGP2, and;Imple...
Sequence the genomes of > 1% of the world population with maximal genetic representation (80 M individuals from > 100 countries);Contribute 50,000 telomere-to-telomere (T2T) phased diploid reference genomes from > 20 countries to a Human Pangenome Project and expand the pangenome reference ...
