<p><b>Copyright information:</b></p><p>Taken from "Gene-resolution analysis of DNA copy number variation using oligonucleotide expression microarrays"</p><p>http://www.biomedcentral.com/1471-2164/8/111</p><p>BMC Genomics 2007;8():111-111.</p><p>Published online 30 Apr 2007</p><p>PMCID:PMC1868757.</p><p></p>r differences at 140 to 228 Mb of chromosome 1, where SK-N-SH/L shows gain while SK-N-SH/G shows normal DNA content. Segmentation analysis of BAC aCGH (A) and graCNV (B) highlight the same region as amplified. log2 copy numbers inferred from CBS are shown as red (SK-N-SH/G) and blue (SK-N-SH/L) lines
<p><b>Copyright information:</b></p><p>Taken from "Oligonucleotide Array Comparative Genomic Hybridi...
Ray (red lines). The three panels represent three independent replicates of the test sample NA15510 ...
<p><b>(A)</b> Copy number gains (red) and losses (blue) are plotted along the normal genome per each...
<p><b>Copyright information:</b></p><p>Taken from "Gene-resolution analysis of DNA copy number varia...
<p><b>Copyright information:</b></p><p>Taken from "Gene-resolution analysis of DNA copy number varia...
<p><b>Copyright information:</b></p><p>Taken from "Gene-resolution analysis of DNA copy number varia...
<p><b>Copyright information:</b></p><p>Taken from "Gene-resolution analysis of DNA copy number varia...
<p><b>Copyright information:</b></p><p>Taken from "Gene-resolution analysis of DNA copy number varia...
<p><b>Copyright information:</b></p><p>Taken from "Functional profiling and gene expression analysis...
Contains fulltext : 51725.pdf (publisher's version ) (Open Access)Recently, compar...
Whilst the majority of inherited diseases have been found to be caused by single base substitutions,...
Recently, comparative genomic hybridization onto bacterial artificial chromosome (BAC) arrays (array...
Whilst the majority of inherited diseases have been found to be caused by single base substitutions,...
Whilst the majority of inherited diseases have been found to be caused by single base substitutions,...
Genomic amplifications and deletions, the consequence of somatic variation, are a hallmark of human ...
<p><b>Copyright information:</b></p><p>Taken from "Oligonucleotide Array Comparative Genomic Hybridi...
Ray (red lines). The three panels represent three independent replicates of the test sample NA15510 ...
<p><b>(A)</b> Copy number gains (red) and losses (blue) are plotted along the normal genome per each...
<p><b>Copyright information:</b></p><p>Taken from "Gene-resolution analysis of DNA copy number varia...
<p><b>Copyright information:</b></p><p>Taken from "Gene-resolution analysis of DNA copy number varia...
<p><b>Copyright information:</b></p><p>Taken from "Gene-resolution analysis of DNA copy number varia...
<p><b>Copyright information:</b></p><p>Taken from "Gene-resolution analysis of DNA copy number varia...
<p><b>Copyright information:</b></p><p>Taken from "Gene-resolution analysis of DNA copy number varia...
<p><b>Copyright information:</b></p><p>Taken from "Functional profiling and gene expression analysis...
Contains fulltext : 51725.pdf (publisher's version ) (Open Access)Recently, compar...
Whilst the majority of inherited diseases have been found to be caused by single base substitutions,...
Recently, comparative genomic hybridization onto bacterial artificial chromosome (BAC) arrays (array...
Whilst the majority of inherited diseases have been found to be caused by single base substitutions,...
Whilst the majority of inherited diseases have been found to be caused by single base substitutions,...
Genomic amplifications and deletions, the consequence of somatic variation, are a hallmark of human ...
<p><b>Copyright information:</b></p><p>Taken from "Oligonucleotide Array Comparative Genomic Hybridi...
Ray (red lines). The three panels represent three independent replicates of the test sample NA15510 ...
<p><b>(A)</b> Copy number gains (red) and losses (blue) are plotted along the normal genome per each...