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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...
Gardado en:
| Publicado en: | G3 (Bethesda) |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Genetics Society of America
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6829143/ https://ncbi.nlm.nih.gov/pubmed/31455677 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/g3.119.400596 |
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