<p>On the left side, the number of SNPs located in each chromosomal arm is indicated, which were explored by the 100 K microarray. On the right side, the number of genes located in each arm is indicated, which were explored for changes in gene expression by the ST1.0 expression microarray. Each bar represents the percentage of recurrent altered SNPs (left) or deregulated genes (right) common to the 4 cell lines. The chromosomal arms are indicated in the middle column. Arms labeled with asterisks had a mean number of CN-altered SNPs higher and statistically significant (p<0.05, chi-square test) compared with the whole genome means. Arms with a statistically significant deregulated gene enrichment were labeled with “a” (identified with both c...
<div><p>Array-based comparative genomic hybridization (aCGH) is a powerful technique for detecting g...
<p>We selected TOP 20% gene in ICan by Random Walk, each bar represents the number of differential a...
Copy number variations (CNVs) are genomic events where the number of copies of a particular gene var...
<p>The left side shows the explored genome (Mb) in each chromosome arm that was explored with the 50...
<p>Panel A shows the copy number log<sub>2</sub> ratio of SNPs investigated in Chr 5 by the 100 K SN...
a<p>20,741 genes were explored for changes in expression with HG-ST1.0 microarray. On average 7,349 ...
<p>Panel A shows box plots with the distribution of tumors (n = 31) according to the percentage of t...
<p>Chromosomes 6 and 10 shows significantly different copy number losses that are highly correlated ...
<p>Panel A shows the copy number log<sub>2</sub> ratio of SNPs investigated in Chr 3 by the 100 K SN...
<p>Frequency of chromosomal aberrations. Fraction of samples with copy number >2.8 (red bars above b...
AbstractDNA copy number aberrations (CNAs) are genetic alterations common in cancer cells. Their tra...
<p>The frequency of samples with gains (red) and losses (green) is shown at the top. Each gray point...
<p>(A) Comparison of the number of somatic nonsynonymous and splice site mutations. (B) Comparison o...
<p>(A) A dynastic tree illustrating the relationship between mother, daughter, and granddaughter clo...
A large database of copy number profiles from cancer genomes can facilitate the identification of re...
<div><p>Array-based comparative genomic hybridization (aCGH) is a powerful technique for detecting g...
<p>We selected TOP 20% gene in ICan by Random Walk, each bar represents the number of differential a...
Copy number variations (CNVs) are genomic events where the number of copies of a particular gene var...
<p>The left side shows the explored genome (Mb) in each chromosome arm that was explored with the 50...
<p>Panel A shows the copy number log<sub>2</sub> ratio of SNPs investigated in Chr 5 by the 100 K SN...
a<p>20,741 genes were explored for changes in expression with HG-ST1.0 microarray. On average 7,349 ...
<p>Panel A shows box plots with the distribution of tumors (n = 31) according to the percentage of t...
<p>Chromosomes 6 and 10 shows significantly different copy number losses that are highly correlated ...
<p>Panel A shows the copy number log<sub>2</sub> ratio of SNPs investigated in Chr 3 by the 100 K SN...
<p>Frequency of chromosomal aberrations. Fraction of samples with copy number >2.8 (red bars above b...
AbstractDNA copy number aberrations (CNAs) are genetic alterations common in cancer cells. Their tra...
<p>The frequency of samples with gains (red) and losses (green) is shown at the top. Each gray point...
<p>(A) Comparison of the number of somatic nonsynonymous and splice site mutations. (B) Comparison o...
<p>(A) A dynastic tree illustrating the relationship between mother, daughter, and granddaughter clo...
A large database of copy number profiles from cancer genomes can facilitate the identification of re...
<div><p>Array-based comparative genomic hybridization (aCGH) is a powerful technique for detecting g...
<p>We selected TOP 20% gene in ICan by Random Walk, each bar represents the number of differential a...
Copy number variations (CNVs) are genomic events where the number of copies of a particular gene var...