Fig. 3From: Achieving robust somatic mutation detection with deep learning models derived from reference data sets of a cancer samplePerformance comparison on WGS, WES, and AmpliSeq data sets. a F1-score (%) comparison on 21 WGS replicates for SNVs and INDELs. b SNV F1-score (%) comparison on WES and AmpliSeq data sets. Here, the SEQC-WGS-GT50-SpikeWGS10 trained models were used for NeuSomatic and NeuSomatic-SBack to article page