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VarScan: variant detection in massively parallel sequencing of individual and pooled samples
Summary: Massively parallel sequencing technologies hold incredible promise for the study of DNA sequence variation, particularly the identification of variants affecting human disease. The unprecedented throughput and relatively short read lengths of Roche/454, Illumina/Solexa, and other platforms...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2734323/ https://ncbi.nlm.nih.gov/pubmed/19542151 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btp373 |
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