Sentence examples for methods with stable from inspiring English sources

By combining LC-MS/MS methods with stable isotope tracing, flux can be monitored through multiple intermediates in a biosynthetic pathway simultaneously.

The plasma concentrations of glimepiride, metformin, miglitol, and sitagliptin were determined by separate, validated LC MS/MS methods with stable isotope-labeled internal standards (glimepiride-d5, metformin-d6, miglitol-d4, and sitagliptin-d4).

The plasma concentrations of pioglitazone and its active metabolites (M-III, keto derivatives of pioglitazone; and M-IV, hydroxy derivatives of pioglitazone) were simultaneously determined by validated LC MS/MS methods with stable isotope-labeled internal standards (pioglitazone-d4, keto pioglitazone-d4, and hydroxy pioglitazone-d5).

Livni et al. put forward a vanishing component analysis method with stable values, i.e., the VCA method, to solve the generator (i.e., vanishing component) for vanishing ideal of fitting data manifold pattern.

As an example, for Cbf1 data, an RBF SVR without feature selection and with parameters optimized on a grid of size 1620 ran in an hour on a laptop with a 2.3 GHz Intel Core i5 and 4 GB RAM, when the method with Stable LASSO feature selection took only 7 min, and the parameters were optimized on the same grid.

In this paper, we extend the implicit-explicit (IMEX) methods of Peer type recently developed by Lang and Hundsdorfer (2017) [16] to a broader class of two-step methods that allow the construction of super-convergent IMEX-Peer methods with A-stable implicit part.

The proposed algorithm has three detection methods to end with stable path.

Successful relative and absolute quantitation of signaling peptides can be achieved in a single cell-sized sample using MALDI MS. A combination of appropriate sample preparation methods, analyte labeling with stable isotope techniques, and advanced MALDI MS approaches allows relative and absolute quantitation of analytes in nanoliter volume samples, including single cells (Table 1).

We compare the efficiency of these algorithms to find the fastest method with more stable results.

To asses the prevalence of hmC across different species, a quantitative LC-MS/MS method was implemented with stable isotope-labelled (SIL) internal standards, which were spiked into samples and calibration standards.[ 17] Its presence and concentrations were determined by using both the LC and MS/MS selectivity.

Methods: non-reconstructable patients with stable critical leg ischaemia were divided into three groups.