Table 1.
Feature | Oligonucleotide microarrays | Spotted microarrays |
Typical probe length | 18 – 30 mers | 500 – 1000 base pairs (cDNA) 25 – 100 mers (oligo) |
Spot density | > 500,000 features per slide | ≤ 80,000 spots per slide |
Hybridization Specificity | High specificity | Not as specific with possible cross-hybridization |
Expression levels | Normalized for single-channel system | Ratio-based normalization for dual-channel system |
Advantages | • Large-scale production • Highly reproducible • Detection of alternative splice variants • Precise measurements • Information can still be generated for genes without expression in the reference/control sample |
• Lower costs • Signal amplification is not needed • Independent of genome sequence • Elimination of artifacts from spotting |
Disadvantages | • Expensive • Few producers of necessary equipment and buffers • Difficulty detecting low abundance transcripts |
• Hybridization is dependent upon length of sequences spotted • Labeling efficiency of dyes is an issue • Little information is generated for genes without expression in the reference/control sample • Handling of clones |