Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Taliun, D.; Harris, D. N.; Kessler, M. D.; Carlson, J.; Szpiech, Z. A.; Torres, R.; Gagliano Taliun, S. A.; Corvelo, A.; Gogarten, S. M.; Min Kang, H.; Pitsillides, A. N.; LeFaive, J.; Lee, S.-b.; Tian, X.; Browning, B. L.; Das, S.; Emde, A.-K.; Clarke, W. E.; Loesch, D. P.; Shetty, A. C.; Blackwell, T. W.; Wong, Q.; Aguet, F.; Albert, C.; Alonso, A.; Ardlie, K. G.; Aslibekyan, S.; Auer, P. L.; Barnard, J.; Barr, R. G.; Becker, L. C.; Beer, R. L.; Benjamin, E. J.; Bielak, L. F.; Blangero, J.; Boehnke, M.; Bowden, D. W.; Brody, J. A.; Burchard, E. G.; Cade, B. E.; Casella, J. F.; Chalazan, B. L

doi:10.1101/563866

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bioRxiv · 10.1101/563866

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

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Abstract

Summary paragraphThe Trans-Omics for Precision Medicine (TOPMed) program seeks to elucidate the genetic architecture and disease biology of heart, lung, blood, and sleep disorders, with the ultimate goal of improving diagnosis, treatment, and prevention. The initial phases of the program focus on whole genome sequencing of individuals with rich phenotypic data and diverse backgrounds. Here, we describe TOPMed goals and design as well as resources and early insights from the sequence data. The resources include a variant browser, a genotype imputation panel, and sharing of genomic and phenotypic data via dbGaP. In 53,581 TOPMed samples, >400 million single-nucleotide and insertion/deletion variants were detected by alignment with the reference genome. Additional novel variants are detectable through assembly of unmapped reads and customized analysis in highly variable loci. Among the >400 million variants detected, 97% have frequency <1% and 46% are singletons. These rare variants provide insights into mutational processes and recent human evolutionary history. The nearly complete catalog of genetic variation in TOPMed studies provides unique opportunities for exploring the contributions of rare and non-coding sequence variants to phenotypic variation. Furthermore, combining TOPMed haplotypes with modern imputation methods improves the power and extends the reach of nearly all genome-wide association studies to include variants down to ~0.01% in frequency.

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Taliun, D., Harris, D. N., Kessler, M. D., Carlson, J., Szpiech, Z. A., Torres, R., Gagliano Taliun, S. A., Corvelo, A., Gogarten, S. M., Min Kang, H., Pitsillides, A. N., LeFaive, J., Lee, S.-b., Tian, X., Browning, B. L., Das, S., Emde, A.-K., Clarke, W. E., Loesch, D. P., Shetty, A. C., Blackwell, T. W., Wong, Q., Aguet, F., Albert, C., Alonso, A., Ardlie, K. G., Aslibekyan, S., Auer, P. L., Barnard, J., Barr, R. G., Becker, L. C., Beer, R. L., Benjamin, E. J., Bielak, L. F., Blangero, J., Boehnke, M., Bowden, D. W., Brody, J. A., Burchard, E. G., Cade, B. E., Casella, J. F., Chalazan, B. L. 2019-03-06. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. https://doi.org/10.1101/563866

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