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LmTag: functional-enrichment and imputation-aware tag SNP selection for population-specific genotyping arrays.
Thanh Nguyen, Dat; Hoang Nguyen, Quan; Thuy Duong, Nguyen; Vo, Nam S.
Afiliação
  • Thanh Nguyen D; Center for Biomedical Informatics, Vingroup Big Data Institute, 458 Minh Khai, 10000, Hanoi, Vietnam.
  • Hoang Nguyen Q; Institute for Molecular Bioscience, University of Queensland, st Lucia, QLD 4067, Brisbane, Australia.
  • Thuy Duong N; Center for Biomedical Informatics, Vingroup Big Data Institute, 458 Minh Khai, 10000, Hanoi, Vietnam.
  • Vo NS; Institute of Genome Research, Vietnam Academy of Science and Technology, 18 Hoang Quoc Viet, 10000, Hanoi, Vietnam.
Brief Bioinform ; 23(4)2022 07 18.
Article em En | MEDLINE | ID: mdl-35780383
ABSTRACT
Despite the rapid development of sequencing technology, single-nucleotide polymorphism (SNP) arrays are still the most cost-effective genotyping solutions for large-scale genomic research and applications. Recent years have witnessed the rapid development of numerous genotyping platforms of different sizes and designs, but population-specific platforms are still lacking, especially for those in developing countries. SNP arrays designed for these countries should be cost-effective (small size), yet incorporate key information needed to associate genotypes with traits. A key design principle for most current platforms is to improve genome-wide imputation so that more SNPs not included in the array (imputed SNPs) can be predicted. However, current tag SNP selection methods mostly focus on imputation accuracy and coverage, but not the functional content of the array. It is those functional SNPs that are most likely associated with traits. Here, we propose LmTag, a novel method for tag SNP selection that not only improves imputation performance but also prioritizes highly functional SNP markers. We apply LmTag on a wide range of populations using both public and in-house whole-genome sequencing databases. Our results show that LmTag improved both functional marker prioritization and genome-wide imputation accuracy compared to existing methods. This novel approach could contribute to the next generation genotyping arrays that provide excellent imputation capability as well as facilitate array-based functional genetic studies. Such arrays are particularly suitable for under-represented populations in developing countries or non-model species, where little genomics data are available while investment in genome sequencing or high-density SNP arrays is limited. $\textrm{LmTag}$ is available at https//github.com/datngu/LmTag.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Genômica Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Genômica Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article