Entering edit mode
4.0 years ago
vpsev3
▴
20
I came across this site https://www.centogene.com/diagnostics/whole-genome-sequencing-with-centogenome.html
Are these low sensitivity rates related to an alignment problem?
I was wondering if, for example, PE150bp shotgun sequencing with 30X depth could detect these variants (like a 22q11.3 microduplication) with higher confidence.