<p>Top panels: distributions of alternate nucleotide proportions for on- and off-SNP allele-dependent CTCF binding events. Bottom panels: relationships between average call quality values and alternate nucleotide proportions are depicted using a 2D density estimate (darker regions correspond to higher density.).</p
Total base pairs are represented as dark blue bars; Total nucleotide variation as light blue bars; i...
<p>(A) The frequency of different SNP types; (B) different SNPtypes in coding sequence (CDS)-nosyn, ...
Cumulative frequencies of sizes of validated and non-validated CNV calls using platform specific alg...
<p>A. Flow chart indicating the overall design of the experiment. CTCF binding was identified and qu...
<p>Reads for samples in each homozygous genotype group at QTL rs11935835 were merged (AA and CC, res...
<p>(A) 4,428 SNPs identified by resequencing at as many sites. Y-axis indicates the number of SNPs i...
A) Single major allele calls; B) Double allele calls (DACs); C) Single minor allele calls; D) Missin...
(A) Relative contribution of different chromosomal compartments to total SNP heritability of the ant...
<p>Analysis of the impacts of single nucleotide polymorphisms on the consensus CTCF motif in human G...
A) Single major allele calls; B) Double allele calls (DACs); C) Single minor allele calls; D) Missin...
<p>The x-axis shows the ten transporter categories, and y-axis shows the corresponding value: (A) th...
<p>A. Summary of allele-specific analysis. SNP loci that show significant allele-specific CTCF bindi...
Light shade of the color represents low mutation density; Dark shade represents high mutation densit...
<p>We analyzed allele-specific binding of all ENCODE cell lines with reported normal karyotype that ...
<p>The fraction of the alternative allele is shown as the percent of total SNPS. Panel A shows the a...
Total base pairs are represented as dark blue bars; Total nucleotide variation as light blue bars; i...
<p>(A) The frequency of different SNP types; (B) different SNPtypes in coding sequence (CDS)-nosyn, ...
Cumulative frequencies of sizes of validated and non-validated CNV calls using platform specific alg...
<p>A. Flow chart indicating the overall design of the experiment. CTCF binding was identified and qu...
<p>Reads for samples in each homozygous genotype group at QTL rs11935835 were merged (AA and CC, res...
<p>(A) 4,428 SNPs identified by resequencing at as many sites. Y-axis indicates the number of SNPs i...
A) Single major allele calls; B) Double allele calls (DACs); C) Single minor allele calls; D) Missin...
(A) Relative contribution of different chromosomal compartments to total SNP heritability of the ant...
<p>Analysis of the impacts of single nucleotide polymorphisms on the consensus CTCF motif in human G...
A) Single major allele calls; B) Double allele calls (DACs); C) Single minor allele calls; D) Missin...
<p>The x-axis shows the ten transporter categories, and y-axis shows the corresponding value: (A) th...
<p>A. Summary of allele-specific analysis. SNP loci that show significant allele-specific CTCF bindi...
Light shade of the color represents low mutation density; Dark shade represents high mutation densit...
<p>We analyzed allele-specific binding of all ENCODE cell lines with reported normal karyotype that ...
<p>The fraction of the alternative allele is shown as the percent of total SNPS. Panel A shows the a...
Total base pairs are represented as dark blue bars; Total nucleotide variation as light blue bars; i...
<p>(A) The frequency of different SNP types; (B) different SNPtypes in coding sequence (CDS)-nosyn, ...
Cumulative frequencies of sizes of validated and non-validated CNV calls using platform specific alg...