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A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation
Copy number variants (CNVs) create a major source of variation among individuals and populations. Array-based comparative genomic hybridisation (aCGH) is a powerful method used to detect and compare the copy numbers of DNA sequences at high resolution along the genome. In recent years, several infor...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3525224/ https://ncbi.nlm.nih.gov/pubmed/20846932 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1479-7364-4-6-421 |
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