Add to ORKGSUMMARY: Copy number variants (CNVs) are a major source of genetic variation. Comparing CNVs between samples is important in elucidating their potential effects in a wide variety of biological contexts. HD-CNV (hotspot detector for copy number variants) is a tool for downstream analysis of previously identified CNV regions from multiple samples, and it detects recurrent regions by finding cliques in an interval graph generated from the input. It creates a unique graphical representation of the data, as well as summary spreadsheets and UCSC (University of California, Santa Cruz) Genome Browser track files. The interval graph, when viewed with other software or by automated graph analysis, is useful in identifying genomic regions of interest ...
Objective: Most methods to detect copy number variation (CNV) have high false positive rates, especi...
Copy-number variation (CNV) is a major class of genomic variation with potentially important functio...
Copy number variation, as a major source of genetic variation in the human genome, are gains or loss...
Summary: Copy number variants (CNVs) are a major source of genetic variation. Comparing CNVs between...
Summary: Copy number variants (CNVs) are a major source of gen-etic variation. Comparing CNVs betwee...
CNVs (Copy Number Variations) are defined as copy number variations of DNA fragments typically large...
A Summary: Copy number variation (CNV) is a major type of structural genomic variation that is incre...
Copy number variation (CNV) is a major type of structural genomic variation that is increasingly stu...
Copy number variation (CNV) is a prevalent form of critical genetic variation that leads to an abnor...
Copy number variation (CNV) in genomic DNA is linked to a variety of human diseases (including c...
Varying depth of high-throughput sequencing reads along a chromosome makes it possible to observe co...
Copy number Variants (CNVs), which comprise deletions, insertions and inversions of genomic sequence...
Background Detection of copy number variation (CNV) in genes associated with disease is important in...
The next-generation sequencing technology offers a wealth of data resources for the detection of cop...
Recent advances in sequencing technologies provide the means for identifying copy number variation (...
Objective: Most methods to detect copy number variation (CNV) have high false positive rates, especi...
Copy-number variation (CNV) is a major class of genomic variation with potentially important functio...
Copy number variation, as a major source of genetic variation in the human genome, are gains or loss...
Summary: Copy number variants (CNVs) are a major source of genetic variation. Comparing CNVs between...
Summary: Copy number variants (CNVs) are a major source of gen-etic variation. Comparing CNVs betwee...
CNVs (Copy Number Variations) are defined as copy number variations of DNA fragments typically large...
A Summary: Copy number variation (CNV) is a major type of structural genomic variation that is incre...
Copy number variation (CNV) is a major type of structural genomic variation that is increasingly stu...
Copy number variation (CNV) is a prevalent form of critical genetic variation that leads to an abnor...
Copy number variation (CNV) in genomic DNA is linked to a variety of human diseases (including c...
Varying depth of high-throughput sequencing reads along a chromosome makes it possible to observe co...
Copy number Variants (CNVs), which comprise deletions, insertions and inversions of genomic sequence...
Background Detection of copy number variation (CNV) in genes associated with disease is important in...
The next-generation sequencing technology offers a wealth of data resources for the detection of cop...
Recent advances in sequencing technologies provide the means for identifying copy number variation (...
Objective: Most methods to detect copy number variation (CNV) have high false positive rates, especi...
Copy-number variation (CNV) is a major class of genomic variation with potentially important functio...
Copy number variation, as a major source of genetic variation in the human genome, are gains or loss...