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A method for finding single-nucleotide polymorphisms with allele frequencies in sequences of deep coverage
BACKGROUND: The allele frequencies of single-nucleotide polymorphisms (SNPs) are needed to select an optimal subset of common SNPs for use in association studies. Sequence-based methods for finding SNPs with allele frequencies may need to handle thousands of sequences from the same genome location (...
| Autores principales: | , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2005
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1239908/ https://www.ncbi.nlm.nih.gov/pubmed/16146575 http://dx.doi.org/10.1186/1471-2105-6-220 |