CNAseg
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Application data |
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| Biological application domain(s) | Structural variants |
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| Created at | Cancer Research UK Cambridge Research Institute |
| Maintained? | Maybe |
Summary: We present a novel approach, called CNAseg, to identify CNAs from second-generation sequencing data. It uses depth of coverage to estimate copy number states and flowcell-to-flowcell variability in cancer and normal samples to control the false positive rate.
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