This variant browser currently shows chromosome locations, alleles, VEP functional annotations, and allele frequencies for 463 million variants observed in 62,784 individuals sequenced in NHLBI's TOPMed program.
The sequencing analysis pipeline consists of two major processes:
If you have a question about this website, contact firstname.lastname@example.org.
Developers: Daniel Taliun and Peter VandeHaar
Acknowledgments: ExAC Developers
The NHLBI Trans-Omics for Precision Medicine (TOPMed) Whole Genome Sequencing Program. BRAVO variant browser: University of Michigan and NHLBI; 2018. Available from: https://bravo.sph.umich.edu/freeze5/hg38/