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RAINBOW: Haplotype-based genome-wide association study using a novel SNP-set method
Difficulty in detecting rare variants is one of the problems in conventional genome-wide association studies (GWAS). The problem is closely related to the complex gene compositions comprising multiple alleles, such as haplotypes. Several single nucleotide polymorphism (SNP) set approaches have been...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Public Library of Science
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7046296/ https://www.ncbi.nlm.nih.gov/pubmed/32059004 http://dx.doi.org/10.1371/journal.pcbi.1007663 |