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Table 3 Recall rate of sequencing based methods on 10 samples

From: A systematic evaluation of copy number alterations detection methods on real SNP array and deep sequencing data

SampleBICseqCNVnormFREECCNVseqrSWsegVarscanCNVnatorRDXplorerReadDepth
3570.90.970.970.820.450.840.6800.06
6203800.970.990.990.920.160.940.150.010.26
K21100560.570.980.740.440.230.270.0500.08
K21500240.910.930.170.740.020.900.010.05
K23100070.9910.890.9600.980.20.010.01
K23100240.9910.880.960.520.970.3600.2
K23100300.990.990.940.960.270.980.480.010.7
AVG0.910.980.80.830.240.840.270.010.19
RS1145270.170.230.740.180.010.170.0100.08
K21100970.390.40.260.3500.30.1800.71
K21500510.570.940.550.520.010.460.040.010.04
AVG0.380.520.520.350.010.310.0800.28