Visualize and explore read alignments to reference sequences. View the coverage of different bases and regions of reference sequences. Investigate quality of aligned reads and identify mismatches. Retrieve feature annotations relative to specific regions of a reference sequence.
|View NGS sequences and annotations (Since R2019b)
- Visualize NGS Data Using Genomics Viewer App
View NGS alignment data for single nucleotide variation in cytochrome p450 gene.