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1 ometrics (i.e., demonstrated using classical least-squares analysis).
2 results were correlated by means of partial least squares analysis.
3 and evaluating their accuracy with a partial least-squares analysis.
4 d rate constants were obtained by nonlinear, least-squares analysis.
7 as been incorporated into a global nonlinear least-squares analysis approach, based upon the Marquard
8 ) and 90 degree angle (alpha)) obtained from least squares analysis are r(C=C) = 1.346(4) A, r(C-C)(r
9 rate constants determined through nonlinear least-squares analysis are also in agreement with protei
10 gle(alpha)) obtained from the combined ED/MW least-squares analysis are r(C-H)(av) = 1.093(6) A, r(C(
13 calibration method, two-dimensional partial least-squares analysis, for calibrating single-particle
14 near-infrared (NIR) spectrometry and partial least-squares analysis has been developed for the noninv
15 ing curvature, parameters estimated from the least-squares analysis have varying degrees of uncertain
16 -component lifetime models used in nonlinear least-squares analysis in which each lifetime component
17 a multivariate curve resolution-alternating least-squares analysis method has been used to character
19 A multilevel, within-group, sparse partial least squares analysis of covariation of microbial, infl
29 The method involves simultaneous (global) least-squares analysis of titrations with Ca(2+), with M
30 bination of simulation and global non-linear least-squares analysis provides support for a binding mo
33 ses and describe novel methods for nonlinear least-squares analysis that overcome these problems.
34 etic algorithm and couples them to a partial least squares analysis to predict cellular function, and
38 mately 465-630 nm) were modeled using linear least squares analysis with individual chromophore spect
39 (1.2 +/- 0.4) x 104 M-1 s-1 using nonlinear least-squares analysis, yielding an equilibrium binding
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