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Structural and conformational requirements for affinity were outlined by NOE NMR and computational methods and suggestions for a pharmacophore model design were provided.
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The results of these case studies have led to improvements to the method and suggestions for further research.
Finally, some concluding remarks, including limitations of the proposed method and suggestions for future work are given.
Jonathan Bollback is thanked for comments and discussions around the posterior mapping method and suggestions for improving the manuscript.
Starting with the vignette in question we present descriptive summaries of students' experiences with the method, their descriptions of the method in action, problems with the method and suggestions for improvement.
We discuss strengths and weaknesses of both methods, and make suggestions for factors to be considered in future bacterial GWAS.
It discusses both compendia and non-compendia methods and provides suggestions to achieve sound, scientific development, and validation for such methods.
The differences between the results of two methods are discussed and suggestions for applying these methods are also provided.
The limitations associated with these methods are discussed, and suggestions are provided for the selection of suitable methods.
Advantages of both methods are concluded and suggestions are given on how to choose control algorithm for different purpose.
This chapter discusses the numerous benefits of CPTED; its approaches, strategies, and methods; basic concepts; and suggestions for how to put the principles to work.
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