<p>For each function <i>f</i>, the bars indicate the percentage (%) of disease mutations that have a greater and than a conservative threshold at 1% false positive rates (FPR). These thresholds are estimated from the null distributions of and on the set of dbSNP neutral data, respectively. *Indicates significant <i>p</i>-value measured as a one-tailed Fisher’s Exact test after Bonferroni correction for multiple hypothesis testing (<i>p</i> < 8.62 ⋅ 10<sup>−4</sup>). The red line indicates the percentage of neutral variants that have greater and which is exactly 1%.</p
<p>Dashed line is 1% nominal significance threshold for LRT for individual regions, dotted line is 5...
<p>Relative biases are plotted as a function of the coefficient of variation . The different curves ...
<p>Columns of graphs refer to G-P maps (<a href="http://www.plosgenetics.org/article/info:doi/10.137...
<p>Percentage of disease variants with prediction scores at the 1% false positive rate threshold in ...
<p>Blue bar represents the percentage of mutations that, among the seven used algorithms, presented ...
<p>Top Row: The proportion of polymorphic sites where a mutant allele represents a change towards th...
<p>Percentages are the proportion of tumors having a mutation within a subtype, e.g. 37% of Bronchio...
<p>The values in the parentheses are the ratio between the false positive rate and the threshold. Th...
<p>The four known mutations were analyzed by non-synonymous single nucleotide polymorphism (nsSNP) p...
<p>Blue bars show the total number of mutations classified as responsible for the disease, while the...
Background/Aims: We consider the situation that multiple genetic variants are underlying a heritable...
a<p>logistic regression model with 1 df test for the correct genetic model.</p>b<p>logistic regressi...
Percentage calculations in “Number of assemblies” column represent the number of assemblies containi...
The error rate was calculated per run as the count of all non-reference calls per mutation type over...
<p>The CNV explains 1% of the phenotypic variation when present in 20% of the population. The CNV ha...
<p>Dashed line is 1% nominal significance threshold for LRT for individual regions, dotted line is 5...
<p>Relative biases are plotted as a function of the coefficient of variation . The different curves ...
<p>Columns of graphs refer to G-P maps (<a href="http://www.plosgenetics.org/article/info:doi/10.137...
<p>Percentage of disease variants with prediction scores at the 1% false positive rate threshold in ...
<p>Blue bar represents the percentage of mutations that, among the seven used algorithms, presented ...
<p>Top Row: The proportion of polymorphic sites where a mutant allele represents a change towards th...
<p>Percentages are the proportion of tumors having a mutation within a subtype, e.g. 37% of Bronchio...
<p>The values in the parentheses are the ratio between the false positive rate and the threshold. Th...
<p>The four known mutations were analyzed by non-synonymous single nucleotide polymorphism (nsSNP) p...
<p>Blue bars show the total number of mutations classified as responsible for the disease, while the...
Background/Aims: We consider the situation that multiple genetic variants are underlying a heritable...
a<p>logistic regression model with 1 df test for the correct genetic model.</p>b<p>logistic regressi...
Percentage calculations in “Number of assemblies” column represent the number of assemblies containi...
The error rate was calculated per run as the count of all non-reference calls per mutation type over...
<p>The CNV explains 1% of the phenotypic variation when present in 20% of the population. The CNV ha...
<p>Dashed line is 1% nominal significance threshold for LRT for individual regions, dotted line is 5...
<p>Relative biases are plotted as a function of the coefficient of variation . The different curves ...
<p>Columns of graphs refer to G-P maps (<a href="http://www.plosgenetics.org/article/info:doi/10.137...