| BMC Bioinformatics BioMed Central Methodology article (2008) | |||||||||||||||
Abstract | |||||||||||||||
| which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Background: False discovery rate (FDR) methods play an important role in analyzing highdimensional data. There are two types of FDR, tail area-based FDR and local FDR, as well as numerous statistical algorithms for estimating or controlling FDR. These differ in terms of underlying test statistics and procedures employed for statistical learning. Results: A unifying algorithm for simultaneous estimation of both local FDR and tail area-based FDR is presented that can be applied to a diverse range of test statistics, including p-values, correlations, z- and t-scores. This approach is semipararametric and is based on a modified Grenander density estimator. For test statistics other than p-values it allows for empirical null modeling, so that dependencies among tests can be taken into account. The inference of the underlying model employs truncated maximum-likelihood estimation, with the cut-off point chosen according to the false non-discovery rate. Conclusion: The proposed procedure generalizes a number of more specialized algorithms and thus offers a common framework for FDR estimation consistent across test statistics and types of FDR. In comparative study the unified approach performs on par with the best competing yet more specialized alternatives. The algorithm is implemented in R in the "fdrtool " package, available under the GNU GPL from | |||||||||||||||
Details der Publikation | |||||||||||||||
| |||||||||||||||