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Sep 17,2026 Blog
What's Hiding in the Half of the Transcriptome That Single-Cell 3′ Sequencing Misses
Full-Length Transcriptome | Mainstream single-cell 3′ sequencing only reads the last stretch of a transcript — enough to count genes, but not enough to see what's written in between. Alternative splicing, fusion breakpoints, mutation sites, and every RNA born without a poly(A) tail all fall outside its reach. This piece looks at what a single primer swap — from oligo-dT to a semi-random primer — brings back into view, and why the missing half of the transcriptome may hold more answers than the half we've been reading all along.
Sep 08,2026 Blog
A data-driven look at eight months of single-cell and spatial multi-omics publications — 126 papers, 3 Nature and 1 Cell flagship papers, and a cumulative impact factor of 1,582.6.