Table 1.

Overview of available platforms for large-scale analysis of DNA methylation

TechnologyApplicationsAdvantagesLimitationsReferences
Illumina bead arrays Methylation polymorphism discovery and analysis Quantitative Requires design of a primer library (Bibikova et al., 2006a; Bibikova et al., 2006b; Fan et al., 2006) 
  Rapid analysis of up to 96 samples Only 1536 sites can be assayed simultaneously  
Affymetrix arrays Whole-genome methylation mapping High feature density Short oligonucleotide probes produce noisier data (Dalma-Weiszhausz et al., 2006; Schumacher et al., 2006; Zhang et al., 2006) 
  Readily available mouse, human and Arabidopsis arrays `Single channel' hybridization  
  Accessible to researchers with access to a microarray facility Custom arrays prohibitively expensive  
  Reasonable price   
NimbleGen arrays Whole-genome methylation mapping Long oligonucleotide probes produce cleaner data Lower feature density than Affymetrix (Khulan et al., 2006; Nuwaysir et al., 2002; Weber et al., 2007; Zilberman et al., 2007) 
  `Dual channel' hybridization   
  Inexpensive custom arrays   
  Hybridization available as a service at a reasonable price   
Agilent arrays Large-scale methylation mapping Long oligonucleotide probes produce cleaner data Substantially lower feature density than Affymetrix and NimbleGen (Wolber et al., 2006) 
  `Dual channel' hybridization   
Solexa sequencing Whole-genome methylation mapping Quantitative New technology (Barski et al., 2007; Bentley, 2006) 
 Analysis of imprinted loci Does not require hybridization Requires purchase of an expensive instrument  
  Concurrent genotype information   
TechnologyApplicationsAdvantagesLimitationsReferences
Illumina bead arrays Methylation polymorphism discovery and analysis Quantitative Requires design of a primer library (Bibikova et al., 2006a; Bibikova et al., 2006b; Fan et al., 2006) 
  Rapid analysis of up to 96 samples Only 1536 sites can be assayed simultaneously  
Affymetrix arrays Whole-genome methylation mapping High feature density Short oligonucleotide probes produce noisier data (Dalma-Weiszhausz et al., 2006; Schumacher et al., 2006; Zhang et al., 2006) 
  Readily available mouse, human and Arabidopsis arrays `Single channel' hybridization  
  Accessible to researchers with access to a microarray facility Custom arrays prohibitively expensive  
  Reasonable price   
NimbleGen arrays Whole-genome methylation mapping Long oligonucleotide probes produce cleaner data Lower feature density than Affymetrix (Khulan et al., 2006; Nuwaysir et al., 2002; Weber et al., 2007; Zilberman et al., 2007) 
  `Dual channel' hybridization   
  Inexpensive custom arrays   
  Hybridization available as a service at a reasonable price   
Agilent arrays Large-scale methylation mapping Long oligonucleotide probes produce cleaner data Substantially lower feature density than Affymetrix and NimbleGen (Wolber et al., 2006) 
  `Dual channel' hybridization   
Solexa sequencing Whole-genome methylation mapping Quantitative New technology (Barski et al., 2007; Bentley, 2006) 
 Analysis of imprinted loci Does not require hybridization Requires purchase of an expensive instrument  
  Concurrent genotype information   
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