<p><b>A</b>. Scatter plot for all 84,861 variants that occur both in the NCI-60 and the ESP5400. The x-axis is the ratio of frequencies of variants in the NCI-60 vs. the frequencies of the same variants in the ESP5400. The y-axis is the number of the variants, ordered by the frequency ratio. The boxed “Enriched” variants (in the NCI-60) include 2,792 variants, and the boxed “Depleted” variants numbers 319. Enrichment is defined as the top 2.5% of variants for which the ratio of frequencies is ≥10. Depletion is defined as the bottom 2.5% of variants, for which the ratio of frequencies is ≤0.1. In both A and B, the vertical lines drawn at x = 1 indicate equal frequencies in the NCI-60 and non-cancerous genomes (ESP5400). <b>B</b>. Scatter plo...
<p>The y-axis represents the percentage of variants for the allele frequencies and categories repres...
<p><b>A.</b> Bar graph depicts the frequency of nonsynonymous mutations in SWI/SNF (<i>right</i>; co...
<p><b>A</b>–<b>B</b>. Comparison of the variant allelic frequency of mutations detected using whole ...
<p><b>A</b>. The four categories of protein-function-affecting variants, and their level of occurren...
<p>A. Frequency of variants present in nsp3 (nucleotides 4073–5653). B. Frequency of variants presen...
<p>Boxplots show the CNA frequency distributions among tumor samples in 10 randomly selected cancer ...
<p>(A) Circos plot summarizing all of the genetic data in 30,506 mtDNA sequences. From outside the c...
<p>(A) compares the prevalence with which mutations from a specific cancer type fall within signific...
<p>TCC = tumor cell content (%); VF = variant frequency; AR = amplicon reads</p><p>*: variant observ...
Percentage calculations in “Number of assemblies” column represent the number of assemblies containi...
<p>Nucleotide (DS<sub>nt</sub>, in black) and amino acid diversity scores (DS<sub>aa</sub>, in red) ...
<p>Panel A shows box plots with the distribution of tumors (n = 31) according to the percentage of t...
<p>The boxes span the lower and upper quartile with the median indicated by a red bar; whiskers exte...
Background: The NCI-60 is a panel of 60 diverse human cancer cell lines used by the U.S. National Ca...
<p>Genes containing variants were identified with the <i>disease association panel</i> (<b>A-C</b>) ...
<p>The y-axis represents the percentage of variants for the allele frequencies and categories repres...
<p><b>A.</b> Bar graph depicts the frequency of nonsynonymous mutations in SWI/SNF (<i>right</i>; co...
<p><b>A</b>–<b>B</b>. Comparison of the variant allelic frequency of mutations detected using whole ...
<p><b>A</b>. The four categories of protein-function-affecting variants, and their level of occurren...
<p>A. Frequency of variants present in nsp3 (nucleotides 4073–5653). B. Frequency of variants presen...
<p>Boxplots show the CNA frequency distributions among tumor samples in 10 randomly selected cancer ...
<p>(A) Circos plot summarizing all of the genetic data in 30,506 mtDNA sequences. From outside the c...
<p>(A) compares the prevalence with which mutations from a specific cancer type fall within signific...
<p>TCC = tumor cell content (%); VF = variant frequency; AR = amplicon reads</p><p>*: variant observ...
Percentage calculations in “Number of assemblies” column represent the number of assemblies containi...
<p>Nucleotide (DS<sub>nt</sub>, in black) and amino acid diversity scores (DS<sub>aa</sub>, in red) ...
<p>Panel A shows box plots with the distribution of tumors (n = 31) according to the percentage of t...
<p>The boxes span the lower and upper quartile with the median indicated by a red bar; whiskers exte...
Background: The NCI-60 is a panel of 60 diverse human cancer cell lines used by the U.S. National Ca...
<p>Genes containing variants were identified with the <i>disease association panel</i> (<b>A-C</b>) ...
<p>The y-axis represents the percentage of variants for the allele frequencies and categories repres...
<p><b>A.</b> Bar graph depicts the frequency of nonsynonymous mutations in SWI/SNF (<i>right</i>; co...
<p><b>A</b>–<b>B</b>. Comparison of the variant allelic frequency of mutations detected using whole ...