Cargando…
Using high-density DNA methylation arrays to profile copy number alterations
The integration of genomic and epigenomic data is an increasingly popular approach for studying the complex mechanisms driving cancer development. We have developed a method for evaluating both methylation and copy number from high-density DNA methylation arrays. Comparing copy number data from Infi...
Autores principales: | Feber, Andrew, Guilhamon, Paul, Lechner, Matthias, Fenton, Tim, Wilson, Gareth A, Thirlwell, Christina, Morris, Tiffany J, Flanagan, Adrienne M, Teschendorff, Andrew E, Kelly, John D, Beck, Stephan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4054098/ https://www.ncbi.nlm.nih.gov/pubmed/24490765 http://dx.doi.org/10.1186/gb-2014-15-2-r30 |
Ejemplares similares
-
Comments on: Interpretation of genome-wide infinium methylation data from ligated DNA in formalin-fixed paraffin-embedded paired tumor and normal tissue
por: Thirlwell, Christina, et al.
Publicado: (2012) -
Assessment of RainDrop BS-seq as a method for large-scale, targeted bisulfite sequencing
por: Paul, Dirk S, et al.
Publicado: (2014) -
An optimization framework for unsupervised identification of rare copy number variation from SNP array data
por: Yavaş, Gökhan, et al.
Publicado: (2009) -
Meta-analysis of IDH-mutant cancers identifies EBF1 as an interaction partner for TET2
por: Guilhamon, Paul, et al.
Publicado: (2013) -
Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays
por: Dellinger, Andrew E., et al.
Publicado: (2010)