CNAseg
|
Application data |
|
| Biological application domain(s) | Structural variants |
|---|---|
| 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.
"Error: no local variable "counter" was set." is not a number.
Description
Links
References
To add a reference for CNAseg, enter the PubMed ID in the field below and click 'Add'.
[ edit box ]
Search for "CNAseg" in the SEQanswers forum / BioStar or:
| Web Search | Wiki Sites | Scientific |
|---|---|---|