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Impact of copy number variations burden on coding genome in humans using integrated high resolution arrays
Copy number variations (CNVs) alter the transcriptional and translational levels of genes by disrupting the coding structure and this burden of CNVs seems to be a significant contributor to phenotypic variations. Therefore it was necessary to assess the complexities of CNV burden on the coding genom...
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| Pubblicato in: | Genet Res (Camb) |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Cambridge University Press
2014
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7045015/ https://ncbi.nlm.nih.gov/pubmed/25578402 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S0016672314000202 |
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