Why This Webinar?
Short-read single-cell RNA sequencing excels at gene-level quantification, but often obscures transcript structure, isoform usage, and complex splicing.
This webinar focuses on how long-read sequencing changes what is measurable at the single-cell level, and what it takes to implement these workflows in practice.
What You’ll Learn
By attending, you will gain practical insight into:
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How native single-cell long-read RNA libraries are constructed
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Input requirements and sample quality considerations
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Sequencing performance and accuracy expectations
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Isoform- and splice-aware analysis workflows
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Common failure modes and how to avoid them
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When long-read single-cell approaches are most appropriate
ArgenTag Single-Cell
Long-Read Grant
The winner of the ArgenTag single-cell long-read grant will be announced live during this webinar.
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Yes. All registrants will receive access to the recording.
No. The focus is on workflows, performance, and real data.
Yes. Live Q&A will be included.
No, but familiarity with RNA-seq workflows is helpful.