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.


Genomics ViewerView NGS sequences and annotations


Visualize NGS Data Using Genomics Viewer App

Use the Genomics Viewer app to view NGS alignment data for single nucleotide variation in cytochrome p450 gene.