Add to ORKGSummary: Copy number variants (CNVs) are a major source of gen-etic variation. Comparing CNVs between samples is important in elu-cidating 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 mul-tiple 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 intere...
Genetic variations within the human genome can take many forms, including single-nucleotide polymorp...
SUMMARY: Copy number variation (CNV) is a major type of structural genomic variation that is increas...
<div><p>Copy number variation (CNV) is one of the most prevalent genetic variations in the genome, l...
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 genetic variation. Comparing CNVs between...
Copy number variation (CNV) is a prevalent form of critical genetic variation that leads to an abnor...
Copy-number variation (CNV) is a major class of genomic variation with potentially important functio...
Background Detection of copy number variation (CNV) in genes associated with disease is important in...
Copy number variation (CNV) is a type of genomic structural variation which has been associated with...
Copy number Variants (CNVs), which comprise deletions, insertions and inversions of genomic sequence...
Copy number variation (CNV) is pervasive in the human genome and has been shown to contribute signif...
Recent advances in sequencing technologies provide the means for identifying copy number variation (...
Accurate and efficient genome-wide detection of copy number variants (CNVs) is essential for underst...
CNVs (Copy Number Variations) are defined as copy number variations of DNA fragments typically large...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Genetic variations within the human genome can take many forms, including single-nucleotide polymorp...
SUMMARY: Copy number variation (CNV) is a major type of structural genomic variation that is increas...
<div><p>Copy number variation (CNV) is one of the most prevalent genetic variations in the genome, l...
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 genetic variation. Comparing CNVs between...
Copy number variation (CNV) is a prevalent form of critical genetic variation that leads to an abnor...
Copy-number variation (CNV) is a major class of genomic variation with potentially important functio...
Background Detection of copy number variation (CNV) in genes associated with disease is important in...
Copy number variation (CNV) is a type of genomic structural variation which has been associated with...
Copy number Variants (CNVs), which comprise deletions, insertions and inversions of genomic sequence...
Copy number variation (CNV) is pervasive in the human genome and has been shown to contribute signif...
Recent advances in sequencing technologies provide the means for identifying copy number variation (...
Accurate and efficient genome-wide detection of copy number variants (CNVs) is essential for underst...
CNVs (Copy Number Variations) are defined as copy number variations of DNA fragments typically large...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Genetic variations within the human genome can take many forms, including single-nucleotide polymorp...
SUMMARY: Copy number variation (CNV) is a major type of structural genomic variation that is increas...
<div><p>Copy number variation (CNV) is one of the most prevalent genetic variations in the genome, l...