Technology platform | Advantage | Disadvantage | Clinical application | Reference |
---|---|---|---|---|
qPCR | Low cost and easy to operate; Suitable for mass screening | Low sensitivity and specificity; Inability to detect low concentrations of dd-cfDNA | One of the most used tests | |
dd-PCR | High sensitivity; Capable of precisely detecting minor variations in dd-cfDNA | The procedure is complex and expensive; Unsuitable for widespread application; Requires high-quality samples | Suitable for precise monitoring of dd-cfDNA; Holds considerable predictive value in the early stages of acute rejection | |
NGS | Extremely sensitive; Capable of detecting mutations, methylation, and other alterations in dd-cfDNA | High cost; Complex data processing | Capable of providing a comprehensive analysis of mutations and genomic alterations | |
Genome analysis | Epigenetic changes in cfDNA can be detected | The methodology is complex; Data analysis requiring advanced technical support | Genomic methylation analysis can provide important information about immune response and rejection |