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M(3)-S: a genotype calling method incorporating information from samples with known genotypes
BACKGROUND: A key challenge in analyzing high throughput Single Nucleotide Polymorphism (SNP) arrays is the accurate inference of genotypes for SNPs with low minor allele frequencies. A number of calling algorithms have been developed to infer genotypes for common SNPs, but they are limited in their...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4669649/ https://www.ncbi.nlm.nih.gov/pubmed/26634345 http://dx.doi.org/10.1186/s12859-015-0824-5 |