Sentence examples for molecular test with from inspiring English sources

The molecular test with the new primers improved the sensitivity to 100%.

Clinical studies comparing these two tests and the molecular test with treatment outcome are needed.

Hence, a binary outcome of a molecular test with a predetermined cut-off value can prove advantageous in this regard.

All identified MDR-TB cases should be managed by specialised centres directly upon diagnosis and a second independent molecular test with a different technology should be performed to confirm the rapid diagnosis [ 32– 32].

All relevant vendors at the annual meetings of the ESHRE and the European Society of Human Genetics in 2008 were invited to offer a molecular test with the following requirements: It must be applicable at the single cell level for analysis of the PB1and PB2, and zygotes (for confirmation).

The higher analytical sensitivity of PCR explains the higher detection rates compared to HC2 in samples with low-grade cytological and no histological abnormalities and may be suggestive of the presence of latent HPV infection requiring a molecular test with higher analytical sensitivity.

Insights into the extent to which culture is falsely negative can be gained using molecular tests with a higher predicted diagnostic sensitivity, although both culture and molecular tests are prone to reduced sensitivity from factors such as inadequate sampling, the intermittent presence or low number of organisms in specimens such as blood, and prior administration of antimicrobial therapy [1].

11 Consciousness of this led to the development of molecular tests with higher sensitivity compared to cytology.

Molecular testing with first-line targeted crizotinib treatment in this population resulted in a gain of 0.011 QALY compared with standard care.

Accurate measurement of DNA using quantitative real-time PCR (Q-PCR) techniques is fundamental to many molecular tests with clinical [ 1], environmental [ 2], and forensic applications [ 3].

The diagnosis of JHS/EDS-HT still remains unsupported by molecular testing, with the exception of a very few cases purportedly mutated in COL3A1 and TNXB [ 4– 6].