A new rapid molecular point-of-care assay for

Abstract: objective vaginal dropper infection is the most common therapeutic sexually transmitted infection (STI)in the world.

An accurate pointof-care (PoC)

Molecular testing will enable patients to undergo testing and treatment of vaginal T at a time when they go to a urology medical clinic, community STI clinic, pharmacy or doctor's office.

In this report, we describe a rapid prototype analysis of vaginal T cells used in conjunction with the Atlas io PoC Platform and preliminary validation of its performance using 90 clinical samples.

Methods a method for rapid detection of vaginal caterpillars was designed.

Test, with novel electrochemical end

Point detection, more

The copy area of the vaginal T genome was used as the target for detection.

90 clinical vaginal swab samples were used to verify the performance of the prototype test.

Results The sensitivity and specificity of the method were 95. 5% (42/44)and 95. 7% (44/46)

, Respectively, when using clinical samples for testing.

The physical evidence of the separation of some geographically different vaginal caterpillars indicates the inclusion of the test and the test shows that there is no cross

The reactivity of a set of DNA separated from human DNA or from a common crossreactants.

Conclusion The sensitivity and specificity obtained using this prototype analysis is comparable to the sensitivity and specificity of existing central laboratory nucleic acid amplification tests for screening vaginal T patients.

Objective vaginal dropper infection is the most common therapeutic sexually transmitted infection (STI)in the world.

An accurate pointof-care (PoC)

Molecular testing will enable patients to undergo testing and treatment of vaginal T at a time when they go to a urology medical clinic, community STI clinic, pharmacy or doctor's office.

In this report, we describe a rapid prototype analysis of vaginal T cells used in conjunction with the Atlas io PoC Platform and preliminary validation of its performance using 90 clinical samples.

Methods a method for rapid detection of vaginal caterpillars was designed.

Test, with novel electrochemical end

Point detection, more

The copy area of the vaginal T genome was used as the target for detection.

90 clinical vaginal swab samples were used to verify the performance of the prototype test.

Results The sensitivity and specificity of the method were 95. 5% (42/44)and 95. 7% (44/46)

, Respectively, when using clinical samples for testing.

The physical evidence of the separation of some geographically different vaginal caterpillars indicates the inclusion of the test and the test shows that there is no cross

The reactivity of a set of DNA separated from human DNA or from a common crossreactants.

Conclusion The sensitivity and specificity obtained using this prototype analysis is comparable to the sensitivity and specificity of existing central laboratory nucleic acid amplification tests for screening vaginal T patients.

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