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A Novel Computational Framework to Predict Disease-Related Copy Number Variations by Integrating Multiple Data Sources
Copy number variation (CNV) may contribute to the development of complex diseases. However, due to the complex mechanism of path association and the lack of sufficient samples, understanding the relationship between CNV and cancer remains a major challenge. The unprecedented abundance of CNV, gene,...
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| Vydáno v: | Front Genet |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Frontiers Media S.A.
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8276077/ https://ncbi.nlm.nih.gov/pubmed/34267783 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.696956 |
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