Resolution |
Array-specific, generally 30–100bp |
Single nucleotide |
Coverage |
Limited by sequences on the array; repetitive regions usually masked out |
Limited only by alignability of reads to the genome; increases with read length; many repetitive regions can be covered |
Cost |
$400–$800 per array (1–6 million probes); multiple arrays may be needed for large genomes |
$1000–$2000 per Illumina lane (6–15 million readsprior to alignment) |
Source of platform noise |
Cross-hybridization between probes and non-specific targets |
Some GC-biasmay be present |
Experimental design |
Single- or double-channel, depending on platform |
Single channel |
Cost-effective cases |
Large fraction enriched (broad binding), profiling of selected regions |
Small fraction enriched (sharp binding), large genomes |
Required amount of ChIP DNA |
High (few μg) |
Low (10–50 ng) |
Dynamic range |
Lower detection limit, saturation at high signal |
Not limited |
Amplification |
More required |
Less required; single molecule sequencing without amplification is available |
Multiplexing |
Not possible |
Possible |