bioRxivGeneticsPreprint
Prediction Of Eye, Hair And Skin Color In Admixed Populations Of Latin America
Sagnik PalmaliD, Kaustubh AdhikariiD, Javier Mendoza‐RevillaiD, Macarena Fuentes‐GuajardoiD, Caio César Silva de Cerqueira, Juan Camilo Chacón-DuqueiD, Anood Sohail, Malena Hurtado, Valeria VillegasiD, Vanessa Granja, Claudia Jaramillo, William H. AriasiD, Rodrigo BarqueraiD, Paola EverardoiD, Jorge Gómez‐ValdésiD, Hugo Villamil‐RamíreziD, Tábita HünemeieriD, Virgínia RamalloiD, Rolando González‐JoséiD, Lavínia Schüler‐FacciniiD, María Cátira BortoliniiD, Víctor Acuña-AlonzoiD, Samuel Canizales‐QuinterosiD, Carla GalloiD, Giovanni PolettiiD, , Andrés Ruiz‐LinaresiD
Abstract
We report an evaluation of prediction accuracy for eye, hair and skin pigmentation based on genomic and phenotypic data for over 6,500 admixed Latin Americans (the CANDELA dataset). We examined the impact on prediction accuracy of three main factors: (i) The methods of prediction, including classical statistical methods and machine learning approaches, (ii) The inclusion of non-genetic predictors, continental genetic ancestry and pigmentation SNPs in the prediction models, and (iii) Compared two sets of pigmentation SNPs: the commonly-used HIrisPlex-S set (developed in Europeans) and novel SNP sets we defined here based on genome-wide association results in the CANDELA sample. We find that Random Forest or regression are globally the best performing methods. Although continental genetic ancestry has substantial power for prediction of pigmentation in Latin Americans, the inclusion of pigmentation SNPs increases prediction accuracy considerably, particularly for skin color. For hair and eye color, HIrisPlex-S has a similar performance to the CANDELA-specific prediction SNP sets. However, for skin pigmentation the performance of HIrisPlex-S is markedly lower than the SNP set defined here, including predictions in an independent dataset of Native American data. These results reflect the relatively high variation in hair and eye color among Europeans for whom HIrisPlex-S was developed, whereas their variation in skin pigmentation is comparatively lower. Furthermore, we show that the dataset used in the training of prediction models strongly impacts on the portability of these models across Europeans and Native Americans.
- organism: human
- assay: GWAS summary statistics
- research focus: variant effect prediction
- research focus: gene regulatory network inference
- research focus: benchmarking
- approach: machine learning (classical)
- Citations
- 0
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