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Effective normalization for copy number variation detection from whole genome sequencing
BACKGROUND: Whole genome sequencing enables a high resolution view of the human genome and provides unique insights into genome structure at an unprecedented scale. There have been a number of tools to infer copy number variation in the genome. These tools, while validated, also include a number of...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3481445/ https://ncbi.nlm.nih.gov/pubmed/23134596 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-13-S6-S16 |
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