Unifying cancer and normal RNA sequencing data from different sources

Driven by the recent advances of next generation sequencing (NGS) technologies and an urgent need to decode complex human diseases, a multitude of large-scale studies were conducted recently that have resulted in an unprecedented volume of whole transcriptome sequencing (RNA-seq) data, such as the G...

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Detalles Bibliográficos
Autores principales: Wang, Qingguo, Armenia, Joshua, Zhang, Chao, Penson, Alexander V., Reznik, Ed, Zhang, Liguo, Minet, Thais, Ochoa, Angelica, Gross, Benjamin E., Iacobuzio-Donahue, Christine A., Betel, Doron, Taylor, Barry S., Gao, Jianjiong, Schultz, Nikolaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2018
Materias:
Data Descriptor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903355/
https://www.ncbi.nlm.nih.gov/pubmed/29664468
http://dx.doi.org/10.1038/sdata.2018.61

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903355/
https://www.ncbi.nlm.nih.gov/pubmed/29664468
http://dx.doi.org/10.1038/sdata.2018.61

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