VaDiR: an integrated approach to Variant Detection in RNA

BACKGROUND: Advances in next-generation DNA sequencing technologies are now enabling detailed characterization of sequence variations in cancer genomes. With whole-genome sequencing, variations in coding and non-coding sequences can be discovered. But the cost associated with it is currently limitin...

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Detalles Bibliográficos
Autores principales: Neums, Lisa, Suenaga, Seiji, Beyerlein, Peter, Anders, Sara, Koestler, Devin, Mariani, Andrea, Chien, Jeremy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Technical Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827345/
https://www.ncbi.nlm.nih.gov/pubmed/29267927
http://dx.doi.org/10.1093/gigascience/gix122

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5827345/
https://www.ncbi.nlm.nih.gov/pubmed/29267927
http://dx.doi.org/10.1093/gigascience/gix122

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