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CNVannotator: A Comprehensive Annotation Server for Copy Number Variation in the Human Genome
Copy number variation (CNV) is one of the most prevalent genetic variations in the genome, leading to an abnormal number of copies of moderate to large genomic regions. High-throughput technologies such as next-generation sequencing often identify thousands of CNVs involved in biological or patholog...
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| Autores principales: | , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Public Library of Science
2013
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3828214/ https://ncbi.nlm.nih.gov/pubmed/24244640 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0080170 |
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