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Genetic testing analyzes an individual\u2019s DNA to identify mutations or variants that may be associated with certain genetic conditions or diseases. Image: Pexels\/P. Danilyuk<\/p>\n\tGenetic testing analyzes an individual\u2019s DNA to identify mutations or variants that may be associated with certain genetic conditions or diseases. Image: Pexels\/P. Danilyuk<\/p>\n
Researchers at Baylor College of Medicine<\/a> and the Jan and Dan Duncan Neurological Research Institute<\/a> at Texas Children\u2019s Hospital (Duncan NRI) have created a new way to measure genetic variants in the Genome Aggregation Database (gnomAD), one of the world\u2019s most widely used resources for understanding human genetics.<\/p>\n The work, published in Nature Communications<\/a>, applies a method called local ancestry inference (LAI), which breaks the genome into ancestry-specific segments to provide more accurate insights into genetic differences.<\/p>\n \u201cThis research updates our genomic resources to reflect the full spectrum of genetic variation,\u201d said Dr. Elizabeth Atkinson<\/a>, assistant professor in the Department of Molecular and Human Genetics<\/a> at Baylor and principal investigator at the Duncan NRI. \u201cBy refining allele frequency estimates for admixed populations, we can improve the accuracy of genetic diagnoses and reduce the risk of misclassification \u2014 ultimately benefitting patients across all backgrounds.\u201d<\/p>\n The study represents a major step forward in the field of genetic testing and personalized medicine. Atkinson is the senior author of the study, and Pragati Kore<\/a>, graduate student in molecular and human genetics at Baylor, and Dr. Michael Wilso<\/a>n, senior associate computational biologist at Broad Institute, are co-first authors.<\/p>\n Genetic testing is a powerful tool for diagnosing disease. If genetic variants are common in the general population, they are more likely to be benign. However, estimates for most population frequencies are based on averages across large groups. For people whose genetic background reflects ancestry from multiple continents, such as those classified as African\/African American or Latino\/Admixed American in gnomAD, this \u201caggregate\u201d approach can mask important differences between their ancestral components.<\/p>\n Atkinson\u2019s team applied local ancestry inference (LAI) to address this problem. Instead of looking at the genome as a whole, LAI breaks it down into segments tracing back to different continental ancestries (for example, African, European or Indigenous American). The team then calculated how common each variant is within each ancestry segment. This revealed that many variants thought to be rare in global data are common in certain ancestry backgrounds.<\/p>\n These differences are not just academic,\u201d Atkinson said. \u201cThey have clinical consequences.\u201d<\/p>\n Her team found that in the African\/African American and Latino\/Admixed American groups, more than 80% of genetic sites had a higher frequency in at least one ancestry-specific tract than previously reported. In some cases, this pushes the variant above a key clinical threshold used by the American College of Medical Genetics and Genomics to classify a variant as benign. This could lead to a more accurate reclassification of variants that might otherwise be misinterpreted.<\/p>\n The new ancestry-specific data is now publicly available through gnomAD, providing researchers, clinicians and genetic testing laboratories with a more precise tool for interpreting genetic variation.<\/p>\n Ancestry is a complex, and putting a single label on patients is not the most accurate way to diagnose them,\u201d said Atkinson. \u201cWith this research, we are moving toward a more nuanced consideration of ancestry.\u201d<\/p>\n \u00a0<\/p>\n Follow From the Labs on X<\/a>, BlueSky<\/a> and Instagram<\/a>!<\/p>\n![\"\"](\"https:\/\/www.newsbeep.com\/ie\/wp-content\/uploads\/2025\/10\/atkinson-elizabeth-391edd0796de-1-515x515.jpeg\")
<\/a>Dr. Elizabeth Atkinson<\/p>\n