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CNVnator: An approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing
Copy number variation (CNV) in the genome is a complex phenomenon, and not completely understood. We have developed a method, CNVnator, for CNV discovery and genotyping from read-depth (RD) analysis of personal genome sequencing. Our method is based on combining the established mean-shift approach w...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Cold Spring Harbor Laboratory Press
2011
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3106330/ https://ncbi.nlm.nih.gov/pubmed/21324876 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.114876.110 |
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