Expressed HNSCC variants by HPV-status in a well-characterized Michigan cohort

While whole-exome DNA sequencing is the most common technology to study genetic variants in tumors in known exonic regions, RNA-seq is cheaper, covers most of the same exonic regions, and is often more readily available. In this study, we show the utility of mRNA-seq-based variant analysis combined...

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Detalles Bibliográficos
Autores principales: Qin, Tingting, Zhang, Yanxiao, Zarins, Katie R., Jones, Tamara R., Virani, Shama, Peterson, Lisa A., McHugh, Jonathan B., Chepeha, Douglas, Wolf, Gregory T., Rozek, Laura S., Sartor, Maureen A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065423/
https://www.ncbi.nlm.nih.gov/pubmed/30061624
http://dx.doi.org/10.1038/s41598-018-29599-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065423/
https://www.ncbi.nlm.nih.gov/pubmed/30061624
http://dx.doi.org/10.1038/s41598-018-29599-w

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