<p>Data for chromosomes 11, 12 and 19, from twelve G-TL and twenty C-TL are shown. Each column represents a single tumour down through all three panels. Columns are ordered manually based on observed groupings. Each row represents either LOH and DNA copy number (CGH) data, DNA copy number data only (<i>Bcl11b</i> locus) or DNA copy number and mutation data (<i>Ikzf1</i>, <i>Trp53</i> and <i>Pten</i> loci). Locations noted in each row are from GRCm38 positioning.</p
<p>Twelve tumors were analyzed by CGH: ten by cCGH (Panel I, A–J), eight by aCGH (Panel II, B, C, E,...
By accurately describing cancer genomes, we may link genomic mutations to phenotypic effects and eve...
<p>Array CGH results from tumor (A) and constitutional (B) DNA analysis of the affected siblings (pa...
Data are presented for chromosomes 4, 11, 12, 15, and 19 from 48 TLs (95 kcal, n = 27, (A); 65 kcal ...
<p>Copy number variations associated with recombination at the TCRβ, TCRγ, TCRα/δ, Skint, IgH, IgLκ ...
<p><b>Copyright information:</b></p><p>Taken from "Analysis of molecular inversion probe performance...
<p>Panel A shows the major regions of copy number gain (red) or loss (blue) across the genome. The Y...
<p>LOH and copy number changes on chromosome 11. SNP array analysis of neuroblastoma tumor samples a...
The purpose of this study was to use comparative genomic hybridization (CGH) to screen breast tumors...
The purpose of this study was to use comparative genomic hybridization (CGH) to screen breast tumors...
<p><i>TP53</i> mutant tumors can derive oncogenic characteristics that contribute to tumor progressi...
<p>Copy number and LOH analysis of chromosome 17. SNP array analysis of neuroblastoma tumor samples ...
We compare SpaCC (top) to DNAcopy (bottom left) and CNTools (bottom right). Copy number series over ...
<p>DNA copy number profiles of two patients containing a co-amplification of at 8q24.21 (<i>MYC</i>)...
<p>(A) Overall frequency of DNA copy number alterations by aCGH. Frequency analysis measured as a fr...
<p>Twelve tumors were analyzed by CGH: ten by cCGH (Panel I, A–J), eight by aCGH (Panel II, B, C, E,...
By accurately describing cancer genomes, we may link genomic mutations to phenotypic effects and eve...
<p>Array CGH results from tumor (A) and constitutional (B) DNA analysis of the affected siblings (pa...
Data are presented for chromosomes 4, 11, 12, 15, and 19 from 48 TLs (95 kcal, n = 27, (A); 65 kcal ...
<p>Copy number variations associated with recombination at the TCRβ, TCRγ, TCRα/δ, Skint, IgH, IgLκ ...
<p><b>Copyright information:</b></p><p>Taken from "Analysis of molecular inversion probe performance...
<p>Panel A shows the major regions of copy number gain (red) or loss (blue) across the genome. The Y...
<p>LOH and copy number changes on chromosome 11. SNP array analysis of neuroblastoma tumor samples a...
The purpose of this study was to use comparative genomic hybridization (CGH) to screen breast tumors...
The purpose of this study was to use comparative genomic hybridization (CGH) to screen breast tumors...
<p><i>TP53</i> mutant tumors can derive oncogenic characteristics that contribute to tumor progressi...
<p>Copy number and LOH analysis of chromosome 17. SNP array analysis of neuroblastoma tumor samples ...
We compare SpaCC (top) to DNAcopy (bottom left) and CNTools (bottom right). Copy number series over ...
<p>DNA copy number profiles of two patients containing a co-amplification of at 8q24.21 (<i>MYC</i>)...
<p>(A) Overall frequency of DNA copy number alterations by aCGH. Frequency analysis measured as a fr...
<p>Twelve tumors were analyzed by CGH: ten by cCGH (Panel I, A–J), eight by aCGH (Panel II, B, C, E,...
By accurately describing cancer genomes, we may link genomic mutations to phenotypic effects and eve...
<p>Array CGH results from tumor (A) and constitutional (B) DNA analysis of the affected siblings (pa...