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The impact of human copy number variation on gene expression
Recent years have witnessed a flurry of important technological and methodological developments in the discovery and analysis of copy number variations (CNVs), which are increasingly enabling the systematic evaluation of their impact on a broad range of phenotypes from molecular-level (intermediate)...
Tallennettuna:
| Julkaisussa: | Brief Funct Genomics |
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| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4592354/ https://ncbi.nlm.nih.gov/pubmed/25922366 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bfgp/elv017 |
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