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Efficient Approach to Unique Single-Nucleotide Polymorphism Discovery
Single-nucleotide polymorphisms (SNPs) are the most frequently found DNA sequence variations in the human genome. It has been argued that a dense set of SNP markers can be used to identify genetic factors associated with complex disease traits. Because all high-throughput genotyping methods require...
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| Опубликовано в: : | Genome Res |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Cold Spring Harbor Laboratory Press
1999
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC310784/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10330130/ |
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