The American Journal of Human GeneticsGenomicsPeer-reviewed journal article
Characterizing substructure via mixture modeling in large-scale genetic summary statistics
Hayley R StonemaniD, Adelle PriceiD, Nikole Scribner Trout, Riley Lamont, Souha TifouriD, Nikita V. PozdeyeviD, Heather D. Anderson, Christina L. AquilanteiD, Kelsey Arbogast, Christopher H. ArehartiD, Ian M. BrooksiD, Tonya M. BrunettiiD, Judith Brutus-Lestin, Elizabeth E. Burke, Emily M. Casteel, Joanne B. ColeiD, Curtis R. CoughliniD, Kristy CrooksiD, Jacob Crawford, Erin Culver, Michelle N. EdelmanniD, Matthew J. Fisher, Alan W. Franklin, Teresa C. Frye, Hunter George, , Katie M. MarkeriD
Abstract
Genetic summary data are broadly accessible and highly useful including for risk prediction, causal inference, fine mapping, and incorporation of external controls. However, collapsing individual-level data into groups masks intra- and inter-sample heterogeneity, leading to confounding, reduced power, and bias. Ultimately, unaccounted substructure limits summary data usability, especially for understudied or admixed populations. Here, we present Summix2, a comprehensive set of methods and software based on a computationally efficient mixture model to estimate and adjust for substructure in genetic summary data. In extensive simulations and application to public data, Summix2 characterizes finer-scale population structure, identifies ascertainment bias, and identifies potential regions of selection due to local substructure deviation. Summix2 increases the robust use of diverse publicly available summary data resulting in improved and more equitable research.
- assay: GWAS summary statistics
- research focus: fine-mapping
- research focus: benchmarking
- research focus: database / resource
- research focus: software / tool
- approach: statistical model
- Citations
- 3
- FWCI
- 1.76
- Field percentile
- top 19%
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