Copy number variants and overlapping genes associated with each region called in each cell line. (XLSX)</p
Due to the increased accuracy of Copy Number Variable region (CNV) break point mapping, it is now po...
Copy number variation (CNV) is a type of genomic structural variation which has been associated with...
Copy number variation (CNV) has recently gained considerable interest as a source of genetic variati...
<p>Germline variants and copy number variation (CNVs) identified and associated syndromes.</p
<p>(A) <sup>classical</sup>CNVs are identified solely by variation among individuals in the copy num...
Copy number variants (CNVs) were the subject of extensive research in the past years. They are commo...
ABSTR ACT: Copy number variations (CNVs) are gains and losses of genomic sequence between two indivi...
Additional file 2. Figure S1. The cancer predisposition genes (CPGs) located within the pathogenic C...
<p>The first column represents the CNVs detected by CNV-CH in the region 26200000bp–30000000bp of ch...
Copy-number variants (CNVs) form an abundant class of genetic variation with a presumed widespread i...
Copy number variants (CNVs) overlap over 7000 genes, many of which are pivotal in biological pathway...
(A) CNVs can overlap entire genes or fractions of genes. CNVs overlapping with exons of a gene (exon...
*<p>One-sided Fisher's exact p value.</p>**<p>P value Bonferroni-adjusted for 1126 genes overlapping...
duplication/multiplications and identification, but are labor intensive, time consuming, and costly...
Due to the increased accuracy of Copy Number Variable region (CNV) break point mapping, it is now po...
Due to the increased accuracy of Copy Number Variable region (CNV) break point mapping, it is now po...
Copy number variation (CNV) is a type of genomic structural variation which has been associated with...
Copy number variation (CNV) has recently gained considerable interest as a source of genetic variati...
<p>Germline variants and copy number variation (CNVs) identified and associated syndromes.</p
<p>(A) <sup>classical</sup>CNVs are identified solely by variation among individuals in the copy num...
Copy number variants (CNVs) were the subject of extensive research in the past years. They are commo...
ABSTR ACT: Copy number variations (CNVs) are gains and losses of genomic sequence between two indivi...
Additional file 2. Figure S1. The cancer predisposition genes (CPGs) located within the pathogenic C...
<p>The first column represents the CNVs detected by CNV-CH in the region 26200000bp–30000000bp of ch...
Copy-number variants (CNVs) form an abundant class of genetic variation with a presumed widespread i...
Copy number variants (CNVs) overlap over 7000 genes, many of which are pivotal in biological pathway...
(A) CNVs can overlap entire genes or fractions of genes. CNVs overlapping with exons of a gene (exon...
*<p>One-sided Fisher's exact p value.</p>**<p>P value Bonferroni-adjusted for 1126 genes overlapping...
duplication/multiplications and identification, but are labor intensive, time consuming, and costly...
Due to the increased accuracy of Copy Number Variable region (CNV) break point mapping, it is now po...
Due to the increased accuracy of Copy Number Variable region (CNV) break point mapping, it is now po...
Copy number variation (CNV) is a type of genomic structural variation which has been associated with...
Copy number variation (CNV) has recently gained considerable interest as a source of genetic variati...
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