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DEFOR: depth- and frequency-based somatic copy number alteration detector
MOTIVATION: Detection of somatic copy number alterations (SCNAs) using high-throughput sequencing has become popular because of rapid developments in sequencing technology. Existing methods do not perform well in calling SCNAs for the unstable tumor genomes. RESULTS: We developed a new method, DEFOR...
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| Udgivet i: | Bioinformatics |
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| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Oxford University Press
2019
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6761943/ https://ncbi.nlm.nih.gov/pubmed/30860569 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btz170 |
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