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Evaluating the impact of single nucleotide variants on transcription factor binding
Diseases and phenotypes caused by disrupted transcription factor (TF) binding are being identified, but progress is hampered by our limited capacity to predict such functional alterations. Improving predictions may be dependent on expanding the set of bona fide TF binding alterations. Allele-specifi...
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| I publikationen: | Nucleic Acids Res |
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| Huvudupphovsmän: | , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Oxford University Press
2016
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5137422/ https://ncbi.nlm.nih.gov/pubmed/27492288 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkw691 |
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