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
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
BackgroundSequencing errors are key confounding factors for detecting low-frequency genetic variants that are important for cancer molecular diagnosis, treatment, and surveillance using deep next-gene
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