ライフサイエンスコーパス: threshold cycle

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1 regression plot of input copy number versus threshold cycle by using HIV-1 RNA transcripts at copy n

2 d to IRTP assays as the gold standard with a threshold cycle (C(T)) cutoff of 43.

3 Most GII samples positive by EIA had a threshold cycle (C(T)) of <26.5, and 50% of the GII samp

4 RNA qPCR exhibited a significant decrease in threshold cycle (C(T)) time values (C(T) control - C(T)

5 The mean real-time PCR threshold cycle (C(T)) value for specimens with discorda

6 The mean real-time PCR threshold cycle (C(T)) value for specimens with discorda

7 tive by the CDC rRT-PCR by virtue of showing threshold cycle (C(T)) values only with universal InfA a

8 t in clinical samples and EQA samples with a threshold cycle (CT ) value of <30 were detected correct

9 ve quantities of the transgene by taking the threshold cycle (Ct) of both the transgene and an intern

10 se polymerase chain reaction (qRT-PCR)-based threshold cycle (Ct) value and the presence of infectiou

11 An average Threshold Cycle (Ct) value of 15.3 was obtained with S.

12 orming units, and respiratory specimens with threshold cycle (CT) values of <34 typically produced go

13 As expected, WGA products with low (<16.0) threshold cycle (CT) values yielded mostly Cryptosporidi

14 ime polymerase chain reaction (RT-qPCR) uses threshold cycles (Ct values) for measuring relative gene

15 y Prodesse ProFlu+ PCR (a mean real-time PCR threshold cycle [CT] value of 31.9 +/- 2.0), which inclu

16 le data, the standard curve constructed from threshold cycle data had a multiple R2 value of 1.00 and

17 actin gene, the coefficient of variation for threshold cycle data was 1.6%, whereas it increased to 1

18 d curves obtained from band densitometry and threshold cycle data, the standard curve constructed fro

19 The qPCR threshold cycle for direct PCR from whole blood is compa

20 Lower threshold cycles indicate increased mtDNA DAMP content.

21 The relative standard deviation in the threshold cycle number is approximately 0.6%.

22 MtDNA DAMPs were quantified as PCR threshold cycle number.

23 tarting copy numbers were amplified, and the threshold cycle showed an increase for decreasing amount

24 From this defined fluorescence threshold, cycle time (Ct) and the error for both amplic

25 c children, we defined a cutoff point in the threshold cycle value (26.7) that predicts rotavirus-att

26 calculated for each pathogen by plotting the threshold cycle value against the bacterial number (log

27 e Method, for analysis of qPCR data based on threshold cycle values (C q ) and efficiencies of reacti

28 reaction (PCR) amplification showed similar threshold cycle values as those obtained from a commerci

29 ich correlated to the measured difference of threshold cycle values for both probes.

30 ot detect HAdV with either low viral burden (threshold cycle values of >30) or nonrespiratory species

31 eal-time PCR (linear correlation between the threshold cycle versus log DNA copy number, >0.982).

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