DIRECT LS-TA quantifies monocyte-specific gene expression in infection diagnostics, suggesting a cost-effective alternative.
Traditional diagnostic test for differentiating infection has several limitations requiring breakthrough including turn-around time and cost. DIRECT LS-TA provides a reliable way to quantify monocyte-specific gene expression that strongly correlates with gold-standard methods. It is more affordable than single-cell RNA sequencing and can be readily implemented in clinical laboratories using widely available quantitative PCR or digital PCR machines.
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Tang et al. (2026) studied this question.
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