This dataset contains sequencing reads used to characterize systematic errors of IonTorrent PGM sequencer as well as all of the analysis results in separate files.
Sequencing errors are key confounding factors for detecting low-frequency genetic variants that are important for cancer molecular diagnosis, treatment, and surveillance using deep next-generation seq
Additional file 5: FASTA file of the 6 reference sequences. The six reference DNA sequences used in this analysis are found in the corresponding FASTA file. They correspond to the control DNA fragment
Supplementary Tables S1-S5. Table S1. Datasets used. Information provided includes data type, provider, analysis type, target region size, sequencing depth, dilution ratio, and sequencer. Table S2a. D