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CNV-TV: A robust method to discover copy number variation from short sequencing reads
BACKGROUND: Copy number variation (CNV) is an important structural variation (SV) in human genome. Various studies have shown that CNVs are associated with complex diseases. Traditional CNV detection methods such as fluorescence in situ hybridization (FISH) and array comparative genomic hybridizatio...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BioMed Central
2013
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3679874/ https://ncbi.nlm.nih.gov/pubmed/23634703 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-14-150 |
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