3DVizSNP: a tool for rapidly visualizing missense mutations identified in high throughput experiments in iCn3D

BACKGROUND: High throughput experiments in cancer and other areas of genomic research identify large numbers of sequence variants that need to be evaluated for phenotypic impact. While many tools exist to score the likely impact of single nucleotide polymorphisms (SNPs) based on sequence alone, the...

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Detalles Bibliográficos
Autores principales: Sierk, Michael, Ratnayake, Shashikala, Wagle, Manoj M., Chen, Ben, Park, Brian, Wang, Jiyao, Youkharibache, Philippe, Meerzaman, Daoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10251577/
https://www.ncbi.nlm.nih.gov/pubmed/37296383
http://dx.doi.org/10.1186/s12859-023-05370-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10251577/
https://www.ncbi.nlm.nih.gov/pubmed/37296383
http://dx.doi.org/10.1186/s12859-023-05370-5

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