Preprocess sequence read data using various functions. Filter reads based on the quality of sequencing data and trim termini of sequences. Perform barcode matching (demultiplexing) to group samples based on their barcodes. Split merged paired-end sequence data into two separate files. Calculate quality statistics and visualize such information using quality control plots.
Use the Genomics Viewer app to view NGS alignment data for single nucleotide variation in cytochrome p450 gene.