DE detection methods, and showing only false positive rates between 0 and 0.04, and false negative rates between 0.5 and 0.9. For these charts only the equal spike-ins are used as true negatives, and all spike-ins with FC > 1 are used as true positives. A post-summarization loess normalization based on the equal-valued spike-ins was used. The legend is the same as in Figure 5.<p><b>Copyright information:</b></p><p>Taken from "A comprehensive re-analysis of the Golden Spike data: Towards a benchmark for differential expression methods"</p><p>http://www.biomedcentral.com/1471-2105/9/164</p><p>BMC Bioinformatics 2008;9():164-164.</p><p>Published online 26 Mar 2008</p><p>PMCID:PMC2324099.</p><p></p
<p><b>Copyright information:</b></p><p>Taken from "Putative null distributions corresponding to test...
Benchmarking RNA-seq differential expression analysis methods using spike-in and simulated RNA-seq d...
Abstract Background Normalization is an important data preparation step in gene expression analyses,...
Arization and DE detection methods. For these charts only the equal spike-ins are used as true negat...
Rization normalization strategies. For these charts only the equal spike-ins are used as true negati...
Hods, and different sets of true positives. For these charts only the equal spike-ins are used as tr...
Robesets are used as true negatives, genes with FC of 1.2 are used as true positives, and no post-su...
Robesets are used as true negatives, genes with FC of 1.2 are used as true positives, and no post-su...
Lden Spike data, for different subsets of probesets. We show plots for three potential choices of tr...
Abstract Background We provide a re-analysis of the Golden Spike dataset, a first generation "spike-...
<p>a. Comparison of estimated rates of false positive spikes () with actual proportion of false posi...
(a) Observed log2 fold change for spike-in constructed true positives plotted against the expected; ...
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 ...
Benchmarking RNA-seq differential expression analysis methods using spike-in and simulated RNA-seq d...
<p><b>Copyright information:</b></p><p>Taken from "Putative null distributions corresponding to test...
Benchmarking RNA-seq differential expression analysis methods using spike-in and simulated RNA-seq d...
Abstract Background Normalization is an important data preparation step in gene expression analyses,...
Arization and DE detection methods. For these charts only the equal spike-ins are used as true negat...
Rization normalization strategies. For these charts only the equal spike-ins are used as true negati...
Hods, and different sets of true positives. For these charts only the equal spike-ins are used as tr...
Robesets are used as true negatives, genes with FC of 1.2 are used as true positives, and no post-su...
Robesets are used as true negatives, genes with FC of 1.2 are used as true positives, and no post-su...
Lden Spike data, for different subsets of probesets. We show plots for three potential choices of tr...
Abstract Background We provide a re-analysis of the Golden Spike dataset, a first generation "spike-...
<p>a. Comparison of estimated rates of false positive spikes () with actual proportion of false posi...
(a) Observed log2 fold change for spike-in constructed true positives plotted against the expected; ...
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 ...
Benchmarking RNA-seq differential expression analysis methods using spike-in and simulated RNA-seq d...
<p><b>Copyright information:</b></p><p>Taken from "Putative null distributions corresponding to test...
Benchmarking RNA-seq differential expression analysis methods using spike-in and simulated RNA-seq d...
Abstract Background Normalization is an important data preparation step in gene expression analyses,...