Fig. 5From: MetaCNV - a consensus approach to infer accurate copy numbers from low coverage dataPrediction accurateness of MetaCNV and other copy number callers for high coverage data. a and b present the average benchmark results per cancer cell line. SVDetect using matchedNormal could only be performed for HCC1187 and HCC2218, for which matched blood samples were available. c and d show the overall results averaged across all benchmarked cell linesBack to article page