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Characterizing substructure via mixture modeling in large-scale genetic summary statistics.

Hayley R StonemanAdelle PriceNikole Scribner TroutRiley LamontSouha TifourNikita Pozdeyevnull nullKristy R CrooksMeng LinNicholas RafaelsChristopher R GignouxKatie M MarkerAudrey E Hendricks
Published in: bioRxiv : the preprint server for biology (2024)
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.
Keyphrases
  • electronic health record
  • big data
  • genome wide
  • healthcare
  • data analysis
  • copy number
  • emergency department
  • high resolution
  • artificial intelligence
  • risk assessment