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Association test using Copy Number Profile Curves (CONCUR) enhances power in rare copy number variant analysis
Copy number variants (CNVs) are the gain or loss of DNA segments in the genome that can vary in dosage and length. CNVs comprise a large proportion of variation in human genomes and impact health conditions. To detect rare CNV associations, kernel-based methods have been shown to be a powerful tool...
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| Publicat a: | PLoS Comput Biol |
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| Autors principals: | , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Public Library of Science
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7224564/ https://ncbi.nlm.nih.gov/pubmed/32365089 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pcbi.1007797 |
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