From prioritisation to understanding: mechanistic predictions of variant effects
Abstract The widespread application of sequencing technologies, used for example to obtain data from healthy individuals or patient cohorts, has led to the identification of numerous mutations, the effect of which remains largely unclear. Therefore, developing approaches allowing accurate in‐silico...
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| Principais autores: | , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Springer Nature
2018-12-01
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| Serier: | Molecular Systems Biology |
| Online adgang: | https://doi.org/10.15252/msb.20188741 |
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