Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis.
Bo ZhouSteve S HoXianglong ZhangReenal PattniRajini R HaraksinghAlexander E UrbanPublished in: Journal of medical genetics (2018)
CNV analysis using low-coverage WGS is efficient and outperforms the array-based analysis that is currently used for clinical cytogenetics.
Keyphrases