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Each complex was tested for cytotoxicity using Trypan blue staining method and none of them were considerably toxic to rat peritoneal cells up to reasonable concentrations which is a desired character of a biological imaging agent.

As a conclusion, amongst the few existing one-to-one HTs, none is a dense method, and none of the existing dense approaches is a one-to-one projection.

Only 6 studies described random allocation method, and none of them described allocation concealment.

In the selection of meta-analyses based on at most five studies and with large ratios between the study sizes (ratio > 5) 13 (59.1%) of the 22 meta-analyses significant with the DL method were not significant with the HKSJ method and none of the meta-analyses was only significant with the HKSJ method.

The associations of survival time with gender, age, tumor location, tumor size, TNM stage, and the 8 immunohistochemical markers (CK, EMA, NSE, Syn, CgA, CD56, TTF-1 and S-100) were analyzed with nonparametric test (Komolgorov-Smirnov method), and none of them was statistically significant (P < 0.05, two-sided probability)' [see Additional file 1]'.

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However, this correlation is observed for all evaluated methods and none shows a considerably stronger correlation compared to the other four.

All those three true positive cases were detected by long-range PCR methods and none with true negative cases were positive.

However, none of the measures correspond closely to gold standard methods, and none are obviously superior to the others [ 11].

So far, most of the official methods for the determination of mycotoxins in food or feed are single-target analyte methods, and none of them is based on LC-MS/MS.

The lack of replication of epistasis was not dependent on the type of specific test or interaction model, because we tested the six SNPs for multiplicative interaction with the PTPN22 rSNP76601 SNP using several methods and none was positive (not shown).

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