diff --git a/EDAM_dev.owl b/EDAM_dev.owl
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@@ -53760,6 +53760,162 @@ Trim sequences (typically from an automated DNA sequencer) to remove sequence-sp
There are two broad categories of small molecule design techniques when applied to the design of drugs: ligand-based drug design (e.g. ligand similarity) and structure-based drug design (ligand docking) methods. Ligand similarity methods exploit structural similarities to known active ligands, whereas ligand docking methods use the 3D structure of a target protein to predict the binding modes and affinities of ligands to it.
Small molecule design
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+ 1.26
+ The estimation of the power of a test; that is the probability of correctly rejecting the null hypothesis when it is false.
+ Estimation of statistical power
+ Power analysis
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+ Power test
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+ 1.26
+ The prediction of DNA modifications (e.g. N4-methylcytosine and N6-Methyladenine) using, for example, statistical models.
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+ DNA modification prediction
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+ 1.26
+ The analysis and simulation of disease transmission using, for example, statistical methods such as the SIR-model.
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+ Disease transmission analysis
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+ 1.26
+ The correction of p-values from multiple statistical tests to correct for false positives.
+ False discovery rate estimation
+ FDR estimation
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+ Multiple testing correction
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