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At the same time apparent replications have been generated from small samples consisting of as few as 142 cases [ 16].
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The cosecant beams are generated from small and large circular arrays.
Gluten specific T cell clones were generated from small intestinal biopsies of celiac disease patients as described before [8], [11], [12].
The assay is inexpensive, data are available within 24 h and only low numbers of cells are required, allowing results to be generated from small clinical biopsies.
Unfortunately, available data were generated from small and underpowered clinical studies that have showed dissimilar Se and Sp for the same recombinant antigen [ 9].
As our data are generated from small patient populations and these data that are not normally distributed, we used the Mann–Whitney U-test for comparison between non-parametric results.
Sites for tryptic and peptic enzymes were identified with PeptideCutter (at www.expasy.org/tools/peptidecutter). A DQ2-γ-I epitope specific T clone was generated from small intestinal biopsies of a celiac disease patient (DQ2.5) as described before [ 15, 16, 22].
Despite the large size of some groups, some odds ratio estimates were generated from smaller sample strata, which resulted in large confidence intervals and less stable inferences.
Many next-generation sequencing datasets for small RNAs have been generated from the adult rodent and human brains [ 33- 38].
It is important to acknowledge that the results presented in this study were generated from a small number of General Practices within a relatively confined geographical area of metropolitan Adelaide.
If an algorithm prefers to predict a large number of complexes with small average size, the room for the improvement of Sn is very limited, since a very small number of new different complexes will be generated from the small original complexes.
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