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VarCon: An R Package for Retrieving Neighboring Nucleotides of an SNV
Reporting of a single nucleotide variant (SNV) follows the Sequence Variant Nomenclature (http://varnomen.hgvs.org/), using an unambiguous numbering scheme specific for coding and noncoding DNA. However, the corresponding sequence neighborhood of a given SNV, which is required to assess its impact o...
Autores principales: | Ptok, Johannes, Theiss, Stephan, Schaal, Heiner |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691889/ https://www.ncbi.nlm.nih.gov/pubmed/33281441 http://dx.doi.org/10.1177/1176935120976399 |
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