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Variant effect predictions capture some aspects of deep mutational scanning experiments
BACKGROUND: Deep mutational scanning (DMS) studies exploit the mutational landscape of sequence variation by systematically and comprehensively assaying the effect of single amino acid variants (SAVs; also referred to as missense mutations, or non-synonymous Single Nucleotide Variants – missense SNV...
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| Publicat a: | BMC Bioinformatics |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7077003/ https://ncbi.nlm.nih.gov/pubmed/32183714 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-020-3439-4 |
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