<p><b>A</b> Concept of FDR calculation which relies on the availability of a normal tissue replication experiment. <b>B</b> Examples of single nucleotide variations found: A somatic mutation found in all three B16 samples (left), a non-somatic mutation found in all B16 and black6 samples (middle) and a mutation found in only one black6 sample (right); this last variation would cause a raise in the FDR for all somatic mutations with a comparable or worse quality. <b>C</b> Process to generate FDRs for a set of somatic mutations and visualize the results. The FDR distribution is visualized as an average estimated ROC curve with the grey bars giving the 95% confidence interval for the mean in both dimensions at uniformly sampled positions. The ...
<p>A.) Pairwise F<sub>ST</sub> of polymorphic sites. Each patient sample was treated as a population...
Background: Thousands of genes in a genomewide data set are tested against some null hypothesis, for...
<p>The numbers of the significant SNP-phenotype associations at various levels of false discovery ra...
<p><b>A</b> ROC curve for all 131 mutations with a successful validation (either positive or negativ...
*<p>FDR is based on was calculated based on 100 permutations where random sets of genes of same size...
<p>Data of gene mutations which are shown only in one patient are not shown. Raw <i>P</i>-values are...
<p>A) Diagram plotting the number of peptides (left) and PSMs (right) identified with each database ...
<p><b>A</b> The Venn diagram shows the numbers of somatic variations in protein coding exons, found ...
Different percentages (P) of simulated DA features are on rows, while different sample size (SS) val...
<p>Abbreviations: FDR1 (FDR from the pathway analysis performed using physical distance only), FDR2 ...
<p>The figures show SCREEN’s estimations vs. real fdr values for different <i>k</i> values. The numb...
False Discover Rate (FDR) method provides more powerful multiple hypothesis testing criteria than th...
<p>Correlation coefficients with raw P<0.05 were presented as colored boxes. Applying FDR correction...
All genes with potentially deleterious ENU mutations are sorted by their chromosomal position on the...
<p>Panels A, B and C show FNR (%) for sequencing coverage of 10X, 20X and 30X, and panels D, E and F...
<p>A.) Pairwise F<sub>ST</sub> of polymorphic sites. Each patient sample was treated as a population...
Background: Thousands of genes in a genomewide data set are tested against some null hypothesis, for...
<p>The numbers of the significant SNP-phenotype associations at various levels of false discovery ra...
<p><b>A</b> ROC curve for all 131 mutations with a successful validation (either positive or negativ...
*<p>FDR is based on was calculated based on 100 permutations where random sets of genes of same size...
<p>Data of gene mutations which are shown only in one patient are not shown. Raw <i>P</i>-values are...
<p>A) Diagram plotting the number of peptides (left) and PSMs (right) identified with each database ...
<p><b>A</b> The Venn diagram shows the numbers of somatic variations in protein coding exons, found ...
Different percentages (P) of simulated DA features are on rows, while different sample size (SS) val...
<p>Abbreviations: FDR1 (FDR from the pathway analysis performed using physical distance only), FDR2 ...
<p>The figures show SCREEN’s estimations vs. real fdr values for different <i>k</i> values. The numb...
False Discover Rate (FDR) method provides more powerful multiple hypothesis testing criteria than th...
<p>Correlation coefficients with raw P<0.05 were presented as colored boxes. Applying FDR correction...
All genes with potentially deleterious ENU mutations are sorted by their chromosomal position on the...
<p>Panels A, B and C show FNR (%) for sequencing coverage of 10X, 20X and 30X, and panels D, E and F...
<p>A.) Pairwise F<sub>ST</sub> of polymorphic sites. Each patient sample was treated as a population...
Background: Thousands of genes in a genomewide data set are tested against some null hypothesis, for...
<p>The numbers of the significant SNP-phenotype associations at various levels of false discovery ra...