The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Independent filtering increases detection power for high-throughput experiments
Open accessAbstract
With high-dimensional data, variable-by-variable statistical testing is often used to select variables whose behavior differs across conditions. Such an approach requires adjustment for multiple testing, which can result in low statistical power. A two-stage approach that first filters variables by a criterion independent of the test statistic, and then only tests variables which pass the filter, can provide higher power. We show that use of some filter/test statistics pairs presented in the literature may, however, lead to loss of type I error control. We describe other pairs which avoid this problem. In an application to microarray data, we found that gene-by-gene filtering by overall variance followed by a t-test increased the number of discoveries by 50%. We also show that this particular statistic pair induces a lower bound on fold-change among the set of discoveries. Independent filtering—using filter/test pairs that are independent under the null hypothesis but correlated under the alternative—is a general approach that can substantially increase the efficiency of experiments.
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Cites
Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing
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Smyth, G. K. (2004) · Statistical Applications in Genetics and Molecular Biology · doi:10.2202/1544-6115.1027 · Cited by 11,829
The control of the false discovery rate in multiple testing under dependency
Benjamini, Y., & Yekutieli, D. (2001) · The Annals of Statistics · doi:10.1214/aos/1013699998 · Cited by 10,490
Moderated statistical tests for assessing differences in tag abundance
Robinson, M. D., & Smyth, G. K. (2007) · Bioinformatics · doi:10.1093/bioinformatics/btm453 · Cited by 856
Cited by
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
Love, M. I., Huber, W., & Anders, S. (2014) · Genome Biology · doi:10.1186/s13059-014-0550-8 · Cited by 95,106
Self-citationGSVA: gene set variation analysis for microarray and RNA-Seq data
Hänzelmann, S., Castelo, R., & Guinney, J. (2013) · BMC Bioinformatics · doi:10.1186/1471-2105-14-7 · Cited by 15,440
RNA sequencing: the teenage years
Stark, R., Grzelak, M., & Hadfield, J. (2019) · Nature Reviews Genetics · doi:10.1038/s41576-019-0150-2 · Cited by 1,915
Detecting differential usage of exons from RNA-seq data
Anders, S., Reyes, A., & Huber, W. (2012) · Genome Research · doi:10.1101/gr.133744.111 · Cited by 1,545
Self-citationMicrobiome differential abundance methods produce different results across 38 datasets
Nearing, J. T., Douglas, G. M., Hayes, M. G., MacDonald, J., Desai, D. K., Allward, N., Jones, C. M. A., Wright, R. J., Dhanani, A. S., Comeau, A. M., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-28034-z · Cited by 992
Metadata
- Authors
- Bourgon, R., Gentleman, R., & Huber, W.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2010-05-11
- Volume
- 107
- Issue
- 21
- Pages
- 9546-9551
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2058358568
- Cited by
- 740
- References
- 4
- FWCI
- 9.10
- Type
- journal article
- Language
- en
- Open access
- green
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