“…Despite these leaps and bounds in medical technology and diagnostic methodologies, many barriers to standard clinical diagnosis remain, such as physician hesitance to adopt new diagnostic methodologies with small bodies of evidence, slow reimbursement from third-party payers for molecular diagnostic techniques, the need to promptly identify drug-resistant and novel pathogens, the need to diagnose culture-negative infections, the inability to promptly differentiate bacterial and viral respiratory infections, and the need for simple and easy to use testing methods when training technicians [ 24 , 26 , 27 , 59 , 60 ]. In addition to the roadblocks to standard clinical care, further limitations exist for the large variety of resource-limited settings such as low- and middle-income countries (LMICs), the Global South, rural areas, and disaster-stricken regions, including the lack of reliable infrastructure for communication, clean water, and power sources, the tendency for infectious diseases to spread rapidly due to crowding after a natural disaster, lack of access to expensive reagents and devices, lack of trained personnel for complex diagnostic techniques, and increased exposure to disease vectors like insects and livestock [ 25 , 61 , 62 , 63 , 64 ]. Biochemical methods like enzyme-linked immunosorbent assays (ELISA) and molecular diagnostic methods, particularly those utilizing nucleic acid tests (NATs) or nucleic acid amplification tests (NAATs) based on the polymerase chain reaction (PCR) and its many derivatives, have proven to be invaluable in overcoming these obstacles when diagnosing both infectious diseases and non-transmissible conditions in a clinical setting due to their relatively simple operation, quantitative results, molecular-level identification of biomarkers, high sensitivity, and relatively low cost in most cases [ 19 , 24 , 25 , 27 , 28 , 38 , 65 , 66 ].…”