<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ma Y</submitter><funding>National Natural Science Foundation of China</funding><funding>National Research Foundation of Korea</funding><funding>Clinical Medicine Plus X - Young Scholars Project</funding><funding>Innovation Fund for Outstanding Doctoral Candidates of Peking University Health Science Center</funding><pagination>356</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12533355</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>26(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Inclusion of individuals with diverse or admixed genetic ancestries is crucial to discover novel findings that may be missed by genomics analyses rooted solely in European population.&lt;h4>Results&lt;/h4>Here, we present an analysis framework, SPAmix, which is scalable to a large-scale biobank data analysis including hundreds of thousands of admixed individuals and is universally applicable to various types of complex traits including quantitative traits, time-to-event traits, ordinal traits, and longitudinal traits. Since no alternative model is fitted, SPAmix primarily focuses on association p values. For each genetic variant, SPAmix uses genotype data and genetic principal components to estimate individual-specific allele frequency, which is subsequently used to calibrate </pubmed_abstract><journal>Genome biology</journal><pubmed_title>SPAmix: a scalable, accurate, and universal analysis framework for large-scale genetic association studies in admixed populations.</pubmed_title><pmcid>PMC12533355</pmcid><funding_grant_id>62411540239</funding_grant_id><funding_grant_id>82441004</funding_grant_id><funding_grant_id>62273010</funding_grant_id><funding_grant_id>PKU2023LCXQ043</funding_grant_id><funding_grant_id>BMU2025BSS001</funding_grant_id><funding_grant_id>32471202</funding_grant_id><funding_grant_id>2024K2A9A2A0601368311</funding_grant_id><pubmed_authors>Lee S</pubmed_authors><pubmed_authors>Bi W</pubmed_authors><pubmed_authors>Xu P</pubmed_authors><pubmed_authors>Zhou XJ</pubmed_authors><pubmed_authors>Kim H</pubmed_authors><pubmed_authors>Zhang JF</pubmed_authors><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Zhou W</pubmed_authors><pubmed_authors>Mao F</pubmed_authors><pubmed_authors>Xu H</pubmed_authors><pubmed_authors>Miao L</pubmed_authors><pubmed_authors>Xu LL</pubmed_authors><pubmed_authors>Zhang P</pubmed_authors><pubmed_authors>Li Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>SPAmix: a scalable, accurate, and universal analysis framework for large-scale genetic association studies in admixed populations.</name><description>&lt;h4>Background&lt;/h4>Inclusion of individuals with diverse or admixed genetic ancestries is crucial to discover novel findings that may be missed by genomics analyses rooted solely in European population.&lt;h4>Results&lt;/h4>Here, we present an analysis framework, SPAmix, which is scalable to a large-scale biobank data analysis including hundreds of thousands of admixed individuals and is universally applicable to various types of complex traits including quantitative traits, time-to-event traits, ordinal traits, and longitudinal traits. Since no alternative model is fitted, SPAmix primarily focuses on association p values. For each genetic variant, SPAmix uses genotype data and genetic principal components to estimate individual-specific allele frequency, which is subsequently used to calibrate </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-07-15T11:56:06.441Z</modification><creation>2026-07-04T03:12:17.056Z</creation></dates><accession>S-EPMC12533355</accession><cross_references><pubmed>41102819</pubmed><doi>10.1186/s13059-025-03827-9</doi></cross_references></HashMap>