An accessible GenePattern notebook for the copy number variation analysis of Illumina Infinium DNA methylation arrays

Illumina Infinium DNA methylation arrays are a cost-effective technology to measure DNA methylation at CpG sites genome-wide and across cohorts of normal and cancer samples. While copy number alterations are commonly inferred from array-CGH, SNP arrays, or whole-genome DNA sequencing, Illumina Infin...

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Detalles Bibliográficos
Autores principales: Mah, Clarence K., Mesirov, Jill P., Chavez, Lukas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2018
Materias:
Software Tool Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498745/
https://www.ncbi.nlm.nih.gov/pubmed/31105932
http://dx.doi.org/10.12688/f1000research.16338.1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6498745/
https://www.ncbi.nlm.nih.gov/pubmed/31105932
http://dx.doi.org/10.12688/f1000research.16338.1

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