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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...
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| Publicado no: | Cancer Inform |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7691889/ https://ncbi.nlm.nih.gov/pubmed/33281441 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1176935120976399 |
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