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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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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cold Spring Harbor Laboratory Press
2007
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| Assuntos: | |
| Acesso em linha: | 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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