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A Deep Learning Approach for Detecting Copy Number Variation in Next-Generation Sequencing Data
Copy number variants (CNV) are associated with phenotypic variation in several species. However, properly detecting changes in copy numbers of sequences remains a difficult problem, especially in lower quality or lower coverage next-generation sequencing data. Here, inspired by recent applications o...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Genetics Society of America
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829143/ https://www.ncbi.nlm.nih.gov/pubmed/31455677 http://dx.doi.org/10.1534/g3.119.400596 |