Table 1.
Methods | Advantages | Disadvantages | Ref. |
---|---|---|---|
Sequencing | High throughput, massively parallel, amplifying the lowest abundant structures |
Low molecular diversity: nucleic acids only | [17,18] |
NMR | Nondestructive method, minimal sample preparation, quantitative analysis, tissue analysis | Lower sensitivity, low molecular diversity |
[2,14,19] |
MS (LC/GC) | Destructive method, capable of depicting volatile compounds, not fully quantitative, target analysis | Partial molecular diversity, less reproducible | [12,13] |
CE-MS | Relatively lower cost than other methods | - | [20,21] |
HPLC-MS | Extensive molecular diversity, robust | Low sensitivity | [22,23] |
Raman micro spectroscopy | 3D evidence, high throughput, structural information, nondestructive enabling | Low sensitivity than MS and NMR | [24,25] |
Immunochemistry | Low throughput, high specificity | Targeted analysis | [26,27] |
NMR, nuclear magnetic resonance; MS, mass spectrometry; CE, capillary electrophoresis; GC, gas chromatography; HPLC: high pressure liquid chromatography; LC, liquid chromatography.