A comparative study of multi-omics integration tools for cancer driver gene identification and tumour subtyping

Oncogenesis and cancer can arise as a consequence of a wide range of genomic aberrations including mutations, copy number alterations, expression changes and epigenetic modifications encompassing multiple omics layers. Integrating genomic, transcriptomic, proteomic and epigenomic datasets via multi-...

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Detalles Bibliográficos
Autores principales: Sathyanarayanan, Anita, Gupta, Rohit, Thompson, Erik W, Nyholt, Dale R, Bauer, Denis C, Nagaraj, Shivashankar H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Problem Solving Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711266/
https://www.ncbi.nlm.nih.gov/pubmed/31774481
http://dx.doi.org/10.1093/bib/bbz121

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7711266/
https://www.ncbi.nlm.nih.gov/pubmed/31774481
http://dx.doi.org/10.1093/bib/bbz121

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