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.
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curl https://depscope.dev/api/check/conda/r-fcrosFirst published · 2021-05-23 12:55:21.577000+00:00
Last updated · 2026-01-29 14:50:14.930000+00:00