You are here

seqr: Integrated Genomics Viewer (IGV)

Visualizing reads is a good way to increase your confidence in a variant called in exome or genome sequencing data. This tutorial will provide an overview of how to visualize cram alignments in seqr through a browser version of the Integrated Genomics Viewer (IGV). 

For more information, please visit:
seqr: seqr.broadinstitute.org
IGV: https://software.broadinstitute.org/software/igv/