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Dear Nikiana,The most accepted and most commonly used methods are Benjamini Hochberg and the false discovery rates (q-values) by Storey (http://www.pnas.org/content/100/16/9440.full). The latter uses information from the actual distribution of p-values (as the Benjamini, Krieger and Yekutieli method) and therefore requires a certain amount of p-values (at least hundreds) distributed over the entire range (0,1).It is well possible that you get more significant features this way as this method is less conservative. I suggest to compare the output of method 1 to the one from Storey. The output should be similar.Best regardsVeit
2017-10-19 15:27 GMT+02:00 <niki...@gmail.com>:
Hi there,Graphpad offers multiple options to do multiple t-test corrections with the false discovery rate approach:1. Two-stage step-up method of Benjamini, Krieger and Yekutieli2. Original FDR of Benjamini and Hochberg3. Corrected method of Benjamini and YekutieliDepending on which one I use, I have different significant proteins and with the first one I get more significant proteins that with the 2nd one (original FDR). Graphpad 7 has as default the two-stage step-up method of Benjamini, Krieger and Yekutieli. I am wondering whether to use this one or to stick to the conservative originical FDR of Benjamini and Hochberg.Thank you for your help.Nikiana
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