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vipR: variant identification in pooled DNA using R
Motivation: High-throughput-sequencing (HTS) technologies are the method of choice for screening the human genome for rare sequence variants causing susceptibility to complex diseases. Unfortunately, preparation of samples for a large number of individuals is still very cost- and labor intensive. Th...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3117388/ https://ncbi.nlm.nih.gov/pubmed/21685105 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btr205 |
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