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A machine learning framework for genotyping the structural variations with copy number variant
BACKGROUND: Genotyping of structural variation is an important computational problem in next generation sequence data analysis. However, in cancer genomes, the copy number variant(CNV) often coexists with other types of structural variations which significantly reduces the accuracy of the existing g...
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| Publicado no: | BMC Med Genomics |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7450592/ https://ncbi.nlm.nih.gov/pubmed/32854699 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-020-00733-w |
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