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.