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Prioritizing Clinically Relevant Copy Number Variation from Genetic Interactions and Gene Function Data
It is becoming increasingly necessary to develop computerized methods for identifying the few disease-causing variants from hundreds discovered in each individual patient. This problem is especially relevant for Copy Number Variants (CNVs), which can be cheaply interrogated via low-cost hybridizatio...
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| Publicado no: | PLoS One |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4593641/ https://ncbi.nlm.nih.gov/pubmed/26437450 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0139656 |
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