The increasing volume of whole-genome sequence (WGS) and multi-omics data requires new approaches for analysis. As one solution, we have created the cloud-based Analysis Commons, which brings together genotype and phenotype data from multiple studies in a setting that is accessible by multiple investigators. This framework addresses many of the challenges of multicenter WGS analyses, including data-sharing mechanisms, phenotype harmonization, integrated multi-omics analyses, annotation and computational flexibility. In this setting, the computational pipeline facilitates a sequence-to-discovery analysis workflow illustrated here by an analysis of plasma fibrinogen levels in 3,996 individuals from the National Heart, Lung, and Blood Institute (NHLBI) Trans-Omics for Precision Medicine (TOPMed) WGS program. The Analysis Commons represents a novel model for translating WGS resources from a massive quantity of phenotypic and genomic data into knowledge of the determinants of health and disease risk in diverse human populations.
Access optionsAccess options
Rent or Buy article
Get time limited or full article access on ReadCube.
All prices are NET prices.
Subscribe to Journal
Get full journal access for 1 year
only $18.75 per issue
All prices are NET prices.
VAT will be added later in the checkout.
TOPMed. WGS for the TOPMed program was supported by the NHLBI. WGS for 'NHLBI TOPMed: Whole Genome Sequencing and Related Phenotypes in the Framingham Heart Study' (phs000974.v1.p1) and 'NHLBI TOPMed: Genetics of Cardiometabolic Health in the Amish' (phs000956.v1.p1) was performed at the Broad Institute of MIT and Harvard (HHSN268201500014C and 3R01HL121007-01S1 (NHLBI, B.D.M.)). Centralized read mapping and genotype calling, along with variant quality metrics and filtering were provided by the TOPMed Informatics Research Center (3R01HL-117626-02S1). Phenotype harmonization, data management, sample-identity quality control and general study coordination were provided by the TOPMed Data Coordinating Center (3R01HL-120393-02S1 (NHLBI, B.M.P., K.M.R. and S.S.R.)). We gratefully acknowledge the studies and participants who provided biological samples and data for TOPMed. The infrastructure for the Analysis Commons is additionally supported by R01HL105756 (NHLBI, B.M.P.), U01HL130114 (NHLBI, B.M.P.) and 5RC2HL102419 (NHLBI, E.B.).
Old Order Amish Study. This investigation was supported by National Institutes of Health grants R01 HL121007 (NHLBI, B.D.M.), U01 GM074518, U01 HL084756 (NHLBI, J.R.O.), U01 HL137181 (NHLBI, J.R.O.) and K23 GM102678 (NIGMS, J.P.L.), as well as Mid-Atlantic Nutrition and Obesity Research Center grant P30 DK072488 (NIDDK, B.D.M.). We also gratefully acknowledge our Amish liaisons and field workers and the extraordinary cooperation and support of the Amish community.
Framingham Heart Study. The Framingham Heart Study was supported by the NHLBI Framingham Heart Study (contract no. N01-HC-25195 and HHSN268201500001I (NHLBI, R.S.V. and L.A.C.)), Fibrinogen measurement was supported by NIH R01-HL-48157. J.E.H. and A.D.J. were supported by NHLBI Intramural Research Program funds. The views expressed in this manuscript are those of the authors and do not necessarily represent the views of the NHLBI, the National Institutes of Health or the US Department of Health and Human Services.