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Nat Biotechnol ; 42(4): 582-586, 2024 Apr.
Article in English | MEDLINE | ID: mdl-37291427

ABSTRACT

Full-length RNA-sequencing methods using long-read technologies can capture complete transcript isoforms, but their throughput is limited. We introduce multiplexed arrays isoform sequencing (MAS-ISO-seq), a technique for programmably concatenating complementary DNAs (cDNAs) into molecules optimal for long-read sequencing, increasing the throughput >15-fold to nearly 40 million cDNA reads per run on the Sequel IIe sequencer. When applied to single-cell RNA sequencing of tumor-infiltrating T cells, MAS-ISO-seq demonstrated a 12- to 32-fold increase in the discovery of differentially spliced genes.


Subject(s)
High-Throughput Nucleotide Sequencing , RNA Isoforms , DNA, Complementary/genetics , RNA Isoforms/genetics , High-Throughput Nucleotide Sequencing/methods , Protein Isoforms/genetics , Sequence Analysis, RNA/methods , Transcriptome , Gene Expression Profiling/methods , RNA/genetics
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