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Alternative splicing and genetic diversity: silencers are more frequently modified by SNVs associated with alternative exon/intron borders
With the availability of a large amount of genomic data it is expected that the influence of single nucleotide variations (SNVs) in many biological phenomena will be elucidated. Here, we approached the problem of how SNVs affect alternative splicing. First, we observed that SNVs and exonic splicing...
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| Päätekijät: | , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2011
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3130264/ https://ncbi.nlm.nih.gov/pubmed/21398627 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkr081 |
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