Visualization
Visualize alignment of reads to reference sequences
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.
Apps
Genomics Viewer | View NGS sequences and annotations |
Objects
genomicsViewer | Open and add files to Genomics Viewer app programmatically (Since R2024a) |
Functions
addTracks | Add tracks to Genomics Viewer (Since R2024a) |
setReference | Specify reference sequence for Genomics Viewer (Since R2024a) |
close | Close Genomics Viewer app (Since R2024a) |
Topics
- Visualize NGS Data Using Genomics Viewer App
View NGS alignment data for single nucleotide variation in cytochrome p450 gene.