Method | Technique | Advantages of technology | Limitations | Sensibility | Reference |
---|---|---|---|---|---|
Microarray platforms | Direct hybridization with probes present in the platform | Potential scalability; quantitative results; few steps until final results | Needed of specialized professionals and equipment; requires the previous setup of miRNA panel; elevated costs of customized panel | fmol | |
qPCR | miRNA amplification and quantification; results were detected using optical sensors | Widespread technique; quantitative results; few steps until final results | Needed of specialized professionals and equipment; time until final results; requires the previous setup of miRNA panel | fmol | [162] |
Next-generation sequencing | Direct sequencing of miRNAs present in the sample | Quantification of all miRNAs in the sample; high accuracy | Elevated operational cost of analysis; needed of specialized professionals and equipment; time until final results | fmol | |
Northern blot | Hybridization with probes and detected according to their sequences and molecular weight | Widespread technique | Semi-quantitative method; laborious and multiple steps protocol | pmol | |
Isothermal amplification | miRNA amplification and quantification; results were detected using optical sensor | Low-cost technique; potential scalability | Nonspecific background amplification; multiple steps protocol; Scalability using clinical samples | fmol |