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PolyScan: An automatic indel and SNP detection approach to the analysis of human resequencing data
Small insertions and deletions (indels) and single nucleotide polymorphisms (SNPs) are common genetic variants that are thought to be associated with a wide variety of human diseases. Owing to the genome’s size and complexity, manually characterizing each one of these variations in an individual is...
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| Autores principales: | , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Cold Spring Harbor Laboratory Press
2007
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1855178/ https://ncbi.nlm.nih.gov/pubmed/17416743 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.6151507 |
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