期刊
G3-GENES GENOMES GENETICS
卷 6, 期 4, 页码 857-863出版社
GENETICS SOCIETY AMERICA
DOI: 10.1534/g3.115.024596
关键词
genotyping-by-sequencing (GBS); single nucleotide polymorphism (SNP); polyploidy; pipeline; haplotype
Genotyping-by-sequencing (GBS), and related methods, are based on high-throughput short-read sequencing of genomic complexity reductions followed by discovery of single nucleotide polymorphisms (SNPs) within sequence tags. This provides a powerful and economical approach to whole-genome genotyping, facilitating applications in genomics, diversity analysis, and molecular breeding. However, due to the complexity of analyzing large data sets, applications of GBS may require substantial time, expertise, and computational resources. Haplotag, the novel GBS software described here, is freely available, and operates with minimal user-investment on widely available computer platforms. Haplotag is unique in fulfilling the following set of criteria: (1) operates without a reference genome; (2) can be used in a polyploid species; (3) provides a discovery mode, and a production mode; (4) discovers polymorphisms based on a model of tag-level haplotypes within sequenced tags; (5) reports SNPs as well as haplotype-based genotypes; and (6) provides an intuitive visual passport for each inferred locus. Haplotag is optimized for use in a self-pollinating plant species.
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