4.3 Article

LinkImpute: Fast and Accurate Genotype Imputation for Nonmodel Organisms

期刊

G3-GENES GENOMES GENETICS
卷 5, 期 11, 页码 2383-2390

出版社

GENETICS SOCIETY AMERICA
DOI: 10.1534/g3.115.021667

关键词

imputation; SNP; genotyping by sequencing; apple

资金

  1. Genome Canada Bioinformatics and Computational Biology grant
  2. Canada Research Chairs program
  3. National Sciences and Engineering Research Council of Canada
  4. ARS [813490, ARS-0425016] Funding Source: Federal RePORTER

向作者/读者索取更多资源

Obtaining genome-wide genotype data from a set of individuals is the first step in many genomic studies, including genome-wide association and genomic selection. All genotyping methods suffer from some level of missing data, and genotype imputation can be used to fill in the missing data and improve the power of downstream analyses. Model organisms like human and cattle benefit from high-quality reference genomes and panels of reference genotypes that aid in imputation accuracy. In nonmodel organisms, however, genetic and physical maps often are either of poor quality or are completely absent, and there are no panels of reference genotypes available. There is therefore a need for imputation methods designed specifically for nonmodel organisms in which genomic resources are poorly developed and marker order is unreliable or unknown. Here we introduce LinkImpute, a software package based on a k-nearest neighbor genotype imputation method, LD-kNNi, which is designed for unordered markers. No physical or genetic maps are required, and it is designed to work on unphased genotype data from heterozygous species. It exploits the fact that markers useful for imputation often are not physically close to the missing genotype but rather distributed throughout the genome. Using genotyping-by-sequencing data from diverse and heterozygous accessions of apples, grapes, and maize, we compare LD-kNNi with several genotype imputation methods and show that LD-kNNi is fast, comparable in accuracy to the best-existing methods, and exhibits the least bias in allele frequency estimates.

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