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A method for an unbiased estimate of cross-ancestry genetic correlation using individual-level data

Author

Listed:
  • Md. Moksedul Momin

    (University of South Australia
    University of South Australia
    Chattogram Veterinary and Animal Sciences University (CVASU)
    University of South Australia)

  • Jisu Shin

    (University of South Australia
    University of South Australia
    University of Virginia
    University of Virginia)

  • Soohyun Lee

    (National Institute of Animal Science (NIAS))

  • Buu Truong

    (University of South Australia)

  • Beben Benyamin

    (University of South Australia
    University of South Australia
    University of South Australia)

  • S. Hong Lee

    (University of South Australia
    University of South Australia
    University of South Australia)

Abstract

Cross-ancestry genetic correlation is an important parameter to understand the genetic relationship between two ancestry groups. However, existing methods cannot properly account for ancestry-specific genetic architecture, which is diverse across ancestries, producing biased estimates of cross-ancestry genetic correlation. Here, we present a method to construct a genomic relationship matrix (GRM) that can correctly account for the relationship between ancestry-specific allele frequencies and ancestry-specific allelic effects. Through comprehensive simulations, we show that the proposed method outperforms existing methods in the estimations of SNP-based heritability and cross-ancestry genetic correlation. The proposed method is further applied to anthropometric and other complex traits from the UK Biobank data across ancestry groups. For obesity, the estimated genetic correlation between African and European ancestry cohorts is significantly different from unity, suggesting that obesity is genetically heterogenous between these two ancestries.

Suggested Citation

  • Md. Moksedul Momin & Jisu Shin & Soohyun Lee & Buu Truong & Beben Benyamin & S. Hong Lee, 2023. "A method for an unbiased estimate of cross-ancestry genetic correlation using individual-level data," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-36281-x
    DOI: 10.1038/s41467-023-36281-x
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    1. Karoline Kuchenbaecker & Nikita Telkar & Theresa Reiker & Robin G. Walters & Kuang Lin & Anders Eriksson & Deepti Gurdasani & Arthur Gilly & Lorraine Southam & Emmanouil Tsafantakis & Maria Karalefthe, 2019. "The transferability of lipid loci across African, Asian and European cohorts," Nature Communications, Nature, vol. 10(1), pages 1-10, December.
    2. Xuan Zhou & Hae Kyung Im & S. Hong Lee, 2020. "CORE GREML for estimating covariance between random effects in linear mixed models for complex trait analyses," Nature Communications, Nature, vol. 11(1), pages 1-11, December.
    3. Konrad J. Karczewski & Laurent C. Francioli & Grace Tiao & Beryl B. Cummings & Jessica Alföldi & Qingbo Wang & Ryan L. Collins & Kristen M. Laricchia & Andrea Ganna & Daniel P. Birnbaum & Laura D. Gau, 2020. "The mutational constraint spectrum quantified from variation in 141,456 humans," Nature, Nature, vol. 581(7809), pages 434-443, May.
    4. Huwenbo Shi & Steven Gazal & Masahiro Kanai & Evan M. Koch & Armin P. Schoech & Katherine M. Siewert & Samuel S. Kim & Yang Luo & Tiffany Amariuta & Hailiang Huang & Yukinori Okada & Soumya Raychaudhu, 2021. "Population-specific causal disease effect sizes in functionally important regions impacted by selection," Nature Communications, Nature, vol. 12(1), pages 1-15, December.
    5. Najaf Amin & Cornelia M van Duijn & Yurii S Aulchenko, 2007. "A Genomic Background Based Method for Association Analysis in Related Individuals," PLOS ONE, Public Library of Science, vol. 2(12), pages 1-7, December.
    6. Qianqian Zhang & Florian Privé & Bjarni Vilhjálmsson & Doug Speed, 2021. "Improved genetic prediction of complex traits from individual-level data or summary statistics," Nature Communications, Nature, vol. 12(1), pages 1-9, December.
    7. Carlos D. Bustamante & Francisco M. De La Vega & Esteban G. Burchard, 2011. "Genomics for the world," Nature, Nature, vol. 475(7355), pages 163-165, July.
    8. Felix C. Tropf & S. Hong Lee & Renske M. Verweij & Gert Stulp & Peter J. van der Most & Ronald de Vlaming & Andrew Bakshi & Daniel A. Briley & Charles Rahal & Robert Hellpap & Anastasia N. Iliadou & T, 2017. "Hidden heritability due to heterogeneity across seven populations," Nature Human Behaviour, Nature, vol. 1(10), pages 757-765, October.
    9. Aysu Okbay & Jonathan P. Beauchamp & Mark Alan Fontana & James J. Lee & Tune H. Pers & Cornelius A. Rietveld & Patrick Turley & Guo-Bo Chen & Valur Emilsson & S. Fleur W. Meddens & Sven Oskarsson & Jo, 2016. "Genome-wide association study identifies 74 loci associated with educational attainment," Nature, Nature, vol. 533(7604), pages 539-542, May.
    10. Yiming Hu & Qiongshi Lu & Ryan Powles & Xinwei Yao & Can Yang & Fang Fang & Xinran Xu & Hongyu Zhao, 2017. "Leveraging functional annotations in genetic risk prediction for human complex diseases," PLOS Computational Biology, Public Library of Science, vol. 13(6), pages 1-16, June.
    Full references (including those not matched with items on IDEAS)

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