A fold change rank based method is presented to search for genes with changing expression and to detect recurrent chromosomal copy number aberrations. This method may be useful for high-throughput biological data (micro-array, sequencing, ...). Probabilities are associated with genes or probes in the data set and there is no problem of multiple tests when using this method. For array-based comparative genomic hybridization data, segmentation results are obtained by merging the significant probes detected.
copied from cf-staging / r-fcros| Label | Latest Version |
|---|---|
| main | 1.6.1 |
| cf202003 | 1.6.1 |
| cf201901 | 1.5.6 |
| gcc7 | 1.5.6 |
