Table 2.
Technique | Advantages | Limitations |
---|---|---|
Quantitative PCR | High sensitivity and specificity | Quantification of only annotated sequences |
High dynamic range | ||
BEAMing, PAP, COBRA, etc. | Higher sensitivity and specificity than quantitative PCR | Analyses of only predetermined sequences |
Detection of at least 0.01 % altered alleles | ||
Microarray | High throughput | Not suitable for accurate quantification |
Relatively low cost | Low dynamic range | |
Detection of only annotated DNA | High signal-to-noise ratio | |
Cross-hybridization between similar sequences | ||
Next-generation sequencing | High sensitivity and specificity | High cost |
Detection of novel and rare alterations | Need for special equipment and bioinformatics | |
Ability to distinguish similar sequences | Relatively high amounts of starting material | |
Sequence-specific bias |
PCR polymerase chain reaction, BEAMing beads, emulsion, amplification and magnetics, PAP pyrophosphorolysis-activated polymerization, COBRA combined bisulfite restriction analysis