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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...
Gorde:
| Argitaratua izan da: | Sci Rep |
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| Egile Nagusiak: | , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Nature Publishing Group UK
2020
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7319969/ https://ncbi.nlm.nih.gov/pubmed/32591545 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-64353-1 |
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