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Current analysis platforms and methods for detecting copy number variation
Copy number variation (CNV), generated through duplication or deletion events that affect one or more loci, is widespread in the human genomes and is often associated with functional consequences that may include changes in gene expression levels or fusion of genes. Genome-wide association studies i...
Gorde:
| Egile Nagusiak: | , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
American Physiological Society
2013
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3544484/ https://ncbi.nlm.nih.gov/pubmed/23132758 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/physiolgenomics.00082.2012 |
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