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A Shallow Convolutional Learning Network for Classification of Cancers Based on Copy Number Variations
Genomic copy number variations (CNVs) are among the most important structural variations. They are linked to several diseases and cancer types. Cancer is a leading cause of death worldwide. Several studies were conducted to investigate the causes of cancer and its association with genomic changes to...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6806227/ https://www.ncbi.nlm.nih.gov/pubmed/31569801 http://dx.doi.org/10.3390/s19194207 |