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Biology subjects

Marker, K.

Publications and source records attributed to Marker, K..

2 recordsLinked to original sources

A Bias Correction Method for Substructure Estimation with Small Reference Sample Sizes

Reference data are important for accurate estimation of population substructure, yet sufficiently large reference samples are often unavailable for some populations. This limitation is especially important for methods that estimate population substructure from genetic summary data using reference allele frequencies derived from reference samples, such as Summix2. Here, we systematically evaluated how reference sample size for five continental reference groups [African (AFR), East Asian (EAS), European (EUR), Indigenous American (IAM), and South Asian (SAS)] affects Summix2 substructure estimates in simulated Latino-like, African American-like, and Peruvian-like populations, as well as real African American genetic data. We show that small reference sample sizes introduce systematic bias in substructure proportion estimates. We identified a sample size threshold of 150 individuals per reference group for accurate estimates with a mean estimation error below 0.05. We also developed two bias corrections: a simple inverse sample size correction and a flexible power-law correction. The power-law correction provided the greatest reduction in mean estimation error when all reference groups had small reference sample sizes, whereas the simple inverse sample size correction performed better when a single reference group had a small reference sample size. These findings provide practical guidance and bias adjustments for reliable population substructure estimation from genetic summary data, particularly when reference populations have small sample sizes.

genomics↗

A polygenic risk score for breast cancer in U.S. Latinas and Latin-American women

BackgroundOver 180 single nucleotide polymorphisms (SNPs) associated with breast cancer susceptibility have been identified; these SNPs can be combined into polygenic risk scores (PRS) to predict breast cancer risk. Since most SNPs were identified in predominantly European populations, little is known about the performance of PRS in non-Europeans. We tested the performance of a 180-SNP PRS in Latinas, a large ethnic group with variable levels of Indigenous American, European, and African ancestry.\n\nMethodsWe conducted a pooled case-control analysis of U.S. Latinas and Latin-American women (4,658 cases, 7,622 controls). We constructed a 180-SNP PRS consisting of SNPs associated with breast cancer risk (p < 5 x 10-8). We evaluated the association between the PRS and breast cancer risk using multivariable logistic regression and assessed discrimination using area under the receiver operating characteristic curve (AUROC). We also assessed PRS performance across quartiles of Indigenous American genetic ancestry.\n\nResultsOf 180 SNPs tested, 142 showed directionally consistent associations compared with European populations, and 39 were nominally significant (p < 0.05). The PRS was associated with breast cancer risk, with an odds ratio (OR) per standard deviation increment of 1.58 (95% CI 1.52 to 1.64) and AUCROC of 0.63 (95% CI 0.62 to 0.64). The discrimination of the PRS was similar between the top and bottom quartiles of Indigenous American ancestry.\n\nConclusionsThe 180-SNP PRS predicts breast cancer risk in Latinas, with similar performance as reported for Europeans. The performance of the PRS did not vary substantially according to Indigenous American ancestry.

epidemiology↗