When identifying differentially expressed genes between two conditions using human population RNA-seq samples, we found a phenomenon by permutation analysis: two popular bioinformatics methods, DESeq2 and edgeR, have unexpectedly high false discovery rates. Expanding the analysis to limma-voom, NOISeq, dearseq, and Wilcoxon rank-sum test, we found that FDR control is often failed except for the Wilcoxon rank-sum test. Particularly, the actual FDRs of DESeq2 and edgeR sometimes exceed 20% when the target FDR is 5%. Based on these results, for population-level RNA-seq studies with large sample sizes, we recommend the Wilcoxon rank-sum test
<p>The fold changes of DE genes are estimated from real data. The columns correspond to the followin...
AbstractFisher’s exact test is widely used in biomedical research, particularly in genomic profile a...
Controlling the false discovery rate (FDR) is a powerful approach to deal with a large number of hyp...
When identifying differentially expressed genes between two conditions using human population RNA-se...
Motivation: An important property of a valid method for testing for differential expression is that ...
International audienceRNA-seq studies are growing in size and popularity. We provide evidence that t...
Background. A number of algorithms exist for analysing RNA-sequencing data to infer profiles of diff...
Motivation: The standard approach for statistical inference in differential expression (DE) analyses...
High throughput sequencing technologies are supplanting microarrays as the preferred technology for ...
<p>On each curve, we marked the position corresponding to a reported FDR of 10% with a cross. The fo...
Controlling the false discovery rate (FDR) is a powerful approach to deal with a large number of hyp...
In recent years, RNA-seq has become a very competitive alternative to microarrays. In RNA-seq experi...
Motivation: The false discovery rate (fdr) is a key tool for statistical assessment of differential ...
The ordinary-, penalized-, and bootstrap t-test, least squares and best linear unbiased prediction w...
High throughput sequencing technologies are supplanting microarrays as the preferred technology for ...
<p>The fold changes of DE genes are estimated from real data. The columns correspond to the followin...
AbstractFisher’s exact test is widely used in biomedical research, particularly in genomic profile a...
Controlling the false discovery rate (FDR) is a powerful approach to deal with a large number of hyp...
When identifying differentially expressed genes between two conditions using human population RNA-se...
Motivation: An important property of a valid method for testing for differential expression is that ...
International audienceRNA-seq studies are growing in size and popularity. We provide evidence that t...
Background. A number of algorithms exist for analysing RNA-sequencing data to infer profiles of diff...
Motivation: The standard approach for statistical inference in differential expression (DE) analyses...
High throughput sequencing technologies are supplanting microarrays as the preferred technology for ...
<p>On each curve, we marked the position corresponding to a reported FDR of 10% with a cross. The fo...
Controlling the false discovery rate (FDR) is a powerful approach to deal with a large number of hyp...
In recent years, RNA-seq has become a very competitive alternative to microarrays. In RNA-seq experi...
Motivation: The false discovery rate (fdr) is a key tool for statistical assessment of differential ...
The ordinary-, penalized-, and bootstrap t-test, least squares and best linear unbiased prediction w...
High throughput sequencing technologies are supplanting microarrays as the preferred technology for ...
<p>The fold changes of DE genes are estimated from real data. The columns correspond to the followin...
AbstractFisher’s exact test is widely used in biomedical research, particularly in genomic profile a...
Controlling the false discovery rate (FDR) is a powerful approach to deal with a large number of hyp...