Uploaded April 2025 | Updated September 2026, 2 hours ago
PacBio long-read sequencing can sequence full-length transcripts, but the capture of ultra-long transcripts (greater than 15kb) might be limited by typical cDNA synthesis methods. Nick Zomer at Radboud University Medical Center shows how using Samplix Xdrop technology to indirectly capture two genes associated with Usher syndrome type 2A, a genetic disease that results in hearing and vision loss.
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PacBio long-read sequencing can sequence full-length transcripts, but the capture of ultra-long transcripts (greater than 15kb) might be limited by typical cDNA synthesis methods. Nick Zomer at Radboud University Medical Center shows how using Samplix Xdrop technology to indirectly capture two genes associated with Usher syndrome type 2A, a genetic disease that results in hearing and vision loss.
🔬 Subscribe to the PacBio YouTube Channel!
Explore the frontiers of genomics with videos on SMRT sequencing, HiFi reads, and real-world applications from scientists across the globe.
👉 Click here to subscribe now! youtube.com/@PacificBiosciences?sub_confirmation=1
Learn more about PacBio at pacb.com
Legal & Trademarks: Visit pacb.com/legal-and-trademarks










