Table 1.
SN | Test | Description | References |
---|---|---|---|
1 | Serological immunoassays | 1) Rapid diagnostic test (RDT) (detection in 10 to 30 min) 2) Enzyme linked immunosorbent assay (ELISA) (detection in 1 to 5 h) 3) Neutralization assay (detection in 3 to 5 days). |
[8], [12] |
2 | Real time RT-PCR | Real time RT-PCR detection is more sensitive and advantageous over reverse transcriptase (RT-PCR) | [13], [14] |
3 | Super high-speed qRT-PCR (SHRT-PCR) | Special rotating disk used for rotating samples to different set temperatures specific to each step of PCR, reducing the time required for temperature ramp up and ramp down time | [15] |
4 | TaqMan-based RT-PCR | TaqMan probes improve the sensitivity of assays | [13], [16] |
5 | Dual TaqMan probe based RT-PCR | 2 probes specific for different sequences used for reducing the detection time with ultra-sensitivity | [17] |
6 | Multiplex RT-PCR | Four mismatch-tolerant molecular beacons targeting four gene used for detection to overcome the issue of rapid mutation in sequences | [13], [18] |
7 | RT-LAMP | Reverse transcription followed by as loop-mediated isothermal amplification. Abolishes the need of sophisticated instruments like thermal cycler as reaction is possible at single temperature by using water bath. | [10], [19] |
8 | RT-RPA | Reverse transcription followed by Recombinase polymerase amplification (RPA) which is also an isothermal amplification | [11] |
9 | Microarray based detection | Complementary probes coated on wells of plate utilized for detection | [20] |