Copy-number-aware differential analysis of quantitative DNA sequencing data

Developments in microarray and high-throughput sequencing (HTS) technologies have resulted in a rapid expansion of research into epigenomic changes that occur in normal development and in the progression of disease, such as cancer. Not surprisingly, copy number variation (CNV) has a direct effect on...

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Detalles Bibliográficos
Autores principales: Robinson, Mark D., Strbenac, Dario, Stirzaker, Clare, Statham, Aaron L., Song, Jenny, Speed, Terence P., Clark, Susan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2012
Materias:
Method
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514678/
https://www.ncbi.nlm.nih.gov/pubmed/22879430
http://dx.doi.org/10.1101/gr.139055.112

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514678/
https://www.ncbi.nlm.nih.gov/pubmed/22879430
http://dx.doi.org/10.1101/gr.139055.112

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