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CONY: A Bayesian procedure for detecting copy number variations from sequencing read depths
Copy number variations (CNVs) are genomic structural mutations consisting of abnormal numbers of fragment copies. Next-generation sequencing of read-depth signals mirrors these variants. Some tools used to predict CNVs by depth have been published, but most of these tools can be applied to only a sp...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Nature Publishing Group UK
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7319969/ https://www.ncbi.nlm.nih.gov/pubmed/32591545 http://dx.doi.org/10.1038/s41598-020-64353-1 |