<p>(A) Correlations of CNAs levels with patient’s age were analyzed using Pearson’s correlation coefficient. Multiple tests were corrected using the Bonferroni correction. The Bonferroni-corrected <i>P</i>-values were calculated by multiplying the observed (uncorrected) <i>P</i>-values by the number of tested genes. Violet colors indicate Bonferroni-adjusted <i>P-</i>value < 0.05. (B) Unsupervised hierarchical clustering analysis of 15 genes in regions with recurrent (>20%) CNAs was performed to investigate correlations among CNAs levels of 11 genes showing copy number gains on 8q24.21, 8q24.3, 20q11.21, and 20q13.12, and 4 genes showing copy number losses. The numbers on the right side of the figure indicate patient identification number. ...
Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletio...
Copy number variants (CNVs) account for a major proportion of human genetic polymorphism and have be...
Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletio...
Differences between genomes can be due to single nucleotide variants (SNPs), translocations, inversi...
Differences between genomes can be due to single nucleotide variants (SNPs), translocations, inversi...
<p>(A-B) Correlations of log2 ratio of DNA copy number and mRNA fold change (FC) of <i>FHIT</i> (A) ...
<p>Cases are ordered from lowest to highest total CNA count down the left-most column. Lowest counts...
<p>a) Genome view of patient CML002BC. Coverage data are represented as Normalized Log2 Ratios. Indi...
Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletio...
<p>a) Genome view of patient CML001BC analyzed by CEQer and (b) corresponding CGH analysis. c) Genom...
<p>Whole-exome view of patients aCML-002 (a) and CML-CP-003 (b). Coverage data are indicated as Norm...
Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletio...
Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletio...
Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletio...
<p>Chromosomes 6 and 10 shows significantly different copy number losses that are highly correlated ...
Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletio...
Copy number variants (CNVs) account for a major proportion of human genetic polymorphism and have be...
Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletio...
Differences between genomes can be due to single nucleotide variants (SNPs), translocations, inversi...
Differences between genomes can be due to single nucleotide variants (SNPs), translocations, inversi...
<p>(A-B) Correlations of log2 ratio of DNA copy number and mRNA fold change (FC) of <i>FHIT</i> (A) ...
<p>Cases are ordered from lowest to highest total CNA count down the left-most column. Lowest counts...
<p>a) Genome view of patient CML002BC. Coverage data are represented as Normalized Log2 Ratios. Indi...
Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletio...
<p>a) Genome view of patient CML001BC analyzed by CEQer and (b) corresponding CGH analysis. c) Genom...
<p>Whole-exome view of patients aCML-002 (a) and CML-CP-003 (b). Coverage data are indicated as Norm...
Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletio...
Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletio...
Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletio...
<p>Chromosomes 6 and 10 shows significantly different copy number losses that are highly correlated ...
Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletio...
Copy number variants (CNVs) account for a major proportion of human genetic polymorphism and have be...
Copy number variations (CNVs) are genomic regions that have added (duplications) or deleted (deletio...