<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan"</p><p>BMC Bioinformatics 2006;7():25-25.</p><p>Published online 18 Jan 2006</p><p>PMCID:PMC1382255.</p><p></p>op row; case L99-2287), 3 (second row; case L99-2297) and 2 (third row), and uniparental isodisomy of chromosome 14 (fourth row; case X_1054). The x-axis spans chromosomes 1–22 and X. B. Detailed view of microdeletions on chromosome 3 (top row) and 2 (bottom row). The x-axis spans chromosomes 2 and 3
<p>Chromosome 4 is trisomic in three of the strains, so changes in read depth for derived (non JPCM5...
<p>KaryoStudio Detected Regions for NHDF-OX1 (parental fibroblasts) and derived hiPSC lines iPS-OX1-...
*<p>Autosomal Trisomies identified (2,3,13,14,15,16,18,20,22).</p>**<p>One unbalanced translocation ...
<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnorma...
<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnorma...
<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnorma...
<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnorma...
<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnorma...
<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnorma...
<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnorma...
Abstract Background A variety of diseases are caused by chromosomal abnormalities such as aneuploidi...
Microarray analysis has provided significant advances in the diagnosis of conditions resulting from ...
Nces are in orange.<p><b>Copyright information:</b></p><p>Taken from "Precise detection of rearrange...
a) LogR and BAF tracks in chromosomes 1 to 6 from tumour CRUK0034. LogR tracks show LogR values in l...
A fundamental goal of single nucleotide polymorphism (SNP) genotyping is to determine the sharing of...
<p>Chromosome 4 is trisomic in three of the strains, so changes in read depth for derived (non JPCM5...
<p>KaryoStudio Detected Regions for NHDF-OX1 (parental fibroblasts) and derived hiPSC lines iPS-OX1-...
*<p>Autosomal Trisomies identified (2,3,13,14,15,16,18,20,22).</p>**<p>One unbalanced translocation ...
<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnorma...
<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnorma...
<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnorma...
<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnorma...
<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnorma...
<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnorma...
<p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnorma...
Abstract Background A variety of diseases are caused by chromosomal abnormalities such as aneuploidi...
Microarray analysis has provided significant advances in the diagnosis of conditions resulting from ...
Nces are in orange.<p><b>Copyright information:</b></p><p>Taken from "Precise detection of rearrange...
a) LogR and BAF tracks in chromosomes 1 to 6 from tumour CRUK0034. LogR tracks show LogR values in l...
A fundamental goal of single nucleotide polymorphism (SNP) genotyping is to determine the sharing of...
<p>Chromosome 4 is trisomic in three of the strains, so changes in read depth for derived (non JPCM5...
<p>KaryoStudio Detected Regions for NHDF-OX1 (parental fibroblasts) and derived hiPSC lines iPS-OX1-...
*<p>Autosomal Trisomies identified (2,3,13,14,15,16,18,20,22).</p>**<p>One unbalanced translocation ...