AbstractArray comparative genomic hybridization (aCGH) has been widely used to detect copy number variants (CNVs) in both research and clinical settings. A customizable aCGH platform may greatly facilitate copy number analyses in genomic regions with higher-order complexity, such as low-copy repeats (LCRs). Here we present the aCGH analyses focusing on the 45kb LCRs [1] at the NPHP1 region with diverse copy numbers in humans. Also, the interspecies aCGH analysis comparing human and nonhuman primates revealed dynamic copy number transitions of the human 45kb LCR orthologues during primate evolution and therefore shed light on the origin of complexity at this locus. The original aCGH data are available at GEO under GSE73962
AbstractWe used the Affymetrix® Genome-Wide Human SNP Array 6.0 to identify heterospecific markers a...
The rhesus macaque is an abundant species of Old World monkeys and a valuable model organism for bio...
Copy number variants affect both disease and normal phenotypic variation, but those lying within hea...
AbstractArray comparative genomic hybridization (aCGH) has been widely used to detect copy number va...
<p><b>A.</b> UCSC Genome Browser tracks showing the diagram of 358 kb LCRs and 45 kb LCRs on the pro...
AbstractIn order to identify human lineage specific (HLS) copy number differences (CNDs) compared to...
Copy number differences (CNDs), and the concomitant differences in gene number, have contributed sig...
Copy number variations (CNVs) are a significant source of genetic diversity and commonly found in ma...
Despite considerable excitement over the potential functional significance of copy-number variants (...
The rhesus macaque is an abundant species of Old World monkeys and a valuable model organism for bio...
Copy number variants (CNVs), defined as losses and gains of segments of genomic DNA, are a major sou...
BACKGROUND Large-scale high throughput studies using microarray technology have established that cop...
Despite considerable excitement over the potential functional significance of copy-number variants (...
Copy number variants affect both disease and normal phenotypic variation, but those lying within hea...
Over recent years small submicroscopic DNA copy-number variants (CNVs) have been highlighted as an i...
AbstractWe used the Affymetrix® Genome-Wide Human SNP Array 6.0 to identify heterospecific markers a...
The rhesus macaque is an abundant species of Old World monkeys and a valuable model organism for bio...
Copy number variants affect both disease and normal phenotypic variation, but those lying within hea...
AbstractArray comparative genomic hybridization (aCGH) has been widely used to detect copy number va...
<p><b>A.</b> UCSC Genome Browser tracks showing the diagram of 358 kb LCRs and 45 kb LCRs on the pro...
AbstractIn order to identify human lineage specific (HLS) copy number differences (CNDs) compared to...
Copy number differences (CNDs), and the concomitant differences in gene number, have contributed sig...
Copy number variations (CNVs) are a significant source of genetic diversity and commonly found in ma...
Despite considerable excitement over the potential functional significance of copy-number variants (...
The rhesus macaque is an abundant species of Old World monkeys and a valuable model organism for bio...
Copy number variants (CNVs), defined as losses and gains of segments of genomic DNA, are a major sou...
BACKGROUND Large-scale high throughput studies using microarray technology have established that cop...
Despite considerable excitement over the potential functional significance of copy-number variants (...
Copy number variants affect both disease and normal phenotypic variation, but those lying within hea...
Over recent years small submicroscopic DNA copy-number variants (CNVs) have been highlighted as an i...
AbstractWe used the Affymetrix® Genome-Wide Human SNP Array 6.0 to identify heterospecific markers a...
The rhesus macaque is an abundant species of Old World monkeys and a valuable model organism for bio...
Copy number variants affect both disease and normal phenotypic variation, but those lying within hea...