S02E08: Long Reads, Big Impact — The Next Leap in Rare Disease Research In this episode, I sit down with Prof. Christian Gilissen, a pioneer in genome bioinformatics, and Head of Bioinformatics at Radboud University Medical Center, to explore how long-read sequencing is revolutionizing the…
S02E08: Long Reads, Big Impact — The Next Leap in Rare Disease ResearchIn this episode, I sit down with Prof. Christian Gilissen, a pioneer in genome bioinformatics, and Head of Bioinformatics at Radboud University Medical Center, to explore how long-read sequencing is revolutionizing the diagnosis of rare diseases. For patients who’ve endured years of uncertainty, this technology offers newfound hope by uncovering genetic variations previously invisible to traditional methods. 🔍 What We Discuss:paultalks.science