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. Author manuscript; available in PMC: 2011 Oct 12.
Published in final edited form as: Nat Rev Genet. 2009 Sep 8;10(10):669–680. doi: 10.1038/nrg2641

Table 1.

Comparison of ChIP-chip and ChIP-Seq

ChIP-chip ChIP-Seq
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