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m6AVar: a database of functional variants involved in m(6)A modification
Identifying disease-causing variants among a large number of single nucleotide variants (SNVs) is still a major challenge. Recently, N(6)-methyladenosine (m(6)A) has become a research hotspot because of its critical roles in many fundamental biological processes and a variety of diseases. Therefore,...
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| Publicado en: | Nucleic Acids Res |
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| Autores principales: | , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Oxford University Press
2018
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5753261/ https://ncbi.nlm.nih.gov/pubmed/29036329 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkx895 |
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