This paper discusses statistical aspects, such as design, sample size determination, and methods of analyses, that will help add rigor and improve the quality of preclinical studies.
Ways of dealing with this include the use of over-determination methods and methods of obtaining more accurate wavenumbers.
A method for determination and two methods for approximation of the domain of attraction D a (0) of the asymptotically stable zero steady state of an autonomous, ℝ-analytical, discrete dynamical system are presented.
1-Methylhydantoin and its novel nickel II) complex [Ni(H2O 4 1-mhyd)2] were prepared and identified, by elemental analysis, single crystal X-ray determination and MS metH2O 4 1-mhyd
Total plant nitrogen (N) concentration was analysed with Kjeldahl determination and colorimetric method as described by Baethgen and Alley (Baethgen & Alley [1989]).
Factors that may have contributed to this discrepancy include serotype determination and PCR method.
Doubling time was determined as described in the Doubling Time Determination section of Materials and Methods except cultures were grown in SCD -URA) inSCD -URA YPAD to ensure plasminsteadtenance.
These issues include study design and sample size determination, analytical methods and quality control and assurance, treatment of missing data or data below the method's limits of detection, and post-hoc analyses of data from multiple studies.
The details of the procedures for spectral processing and analysis, signal assignment, distance restraints and hydrogen bond restraints determinations, structure calculations, structure analysis, and methods used for checking the quality of the structures are all described in the Supporting Information.
High lift devices including trailing-edge flaps, leading-edge slats or flaps, and methods for determination of maximum lift in the takeoff and landing configurations are considered.
