π Huge thanks to the gnomAD team & collaborators β this is a step toward more equitable & clinically useful population frequency resources.
06.10.2025 18:45 β π 0 π 0 π¬ 0 π 0π Huge thanks to the gnomAD team & collaborators β this is a step toward more equitable & clinically useful population frequency resources.
06.10.2025 18:45 β π 0 π 0 π¬ 0 π 0πThe gnomAD browser is now up and running with LAI data live for both genetic ancestry groups!
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π Explore & download:
β’ Check the new Local Ancestry tab in the gnomAD browser: gnomad.broadinstitute.org
β’ Full LAI VCFs & open-source pipeline: github.com/broadinstitu...
π° Texas Childrenβs press release: www.texaschildrens.org/content/news...
π§ͺ Why it matters:
Traditional allele frequencies can mask ancestry-driven differences in admixed genomes. LAI can help clinicians & researchers:
β’ Refine variant interpretation
β’ Improve carrier & disease prevalence estimates
β’ Identify population-enriched risk variants
β’ ~81% of variants with LAI calls now have an updated gnomAD-wide max frequency (grpmax) β changing how some variants are classified.
β’ Variants once below the 5% ACMG BA1 benign threshold can now exceed it in ancestry-specific tracts β stronger evidence to reclassify VUS β Benign.
π Whatβs new:
β’ For the first time, gnomAD includes haplotype-level allele frequencies for genetically inferred African/African American (n = 20,250) and Admixed American (n = 7,612) genomes.
β’ ~85% & ~78% of variants differ β₯2Γ across ancestry tracts, respectively.
π Weβre excited to share our latest work, now published in Nature Communications β a major update to the Genome Aggregation Database (gnomAD) that improves allele frequency resolution for two gnomAD-defined genetic ancestry groups using local ancestry inference (LAI).
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