Entering edit mode
4.1 years ago
vpsev3
▴
20
Hello,
I wonder if it is possible to detect large deletions or duplications with the NGS and with an acceptable sensitivity rate, such as 22q11.3 microduplication
Because I read that it could be complicated with this technique, like here https://www.longdom.org/open-access/structural-variation-detection-from-next-generation-sequencing-2469-9853-S1-007.pdf
