Happy to present our first incursion into Clinical Genomics. It will not be the last 🙂
Paper published in NAR Genomics and Bioinformatics: OPUSeq simplifies detection of low-frequency DNA variants and uncovers fragmentase-associated artifacts. Alekseenko A, Wang J, Barrett D, Pelechano V. NAR Genom Bioinform. 2022 Jun 27;4(2):lqac048.