High-throughput RNA isoform sequencing using programmed cDNA concatenation
利用程序化 cDNA 串联进行高通量 RNA 同源异构体测序
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作者:Aziz M Al'Khafaji # ,Jonathan T Smith # ,Kiran V Garimella # ,Mehrtash Babadi # ,Victoria Popic # ,Moshe Sade-Feldman ,Michael Gatzen ,Siranush Sarkizova ,Marc A Schwartz ,Emily M Blaum ,Allyson Day ,Maura Costello ,Tera Bowers ,Stacey Gabriel ,Eric Banks ,Anthony A Philippakis ,Genevieve M Boland ,Paul C Blainey ,Nir Hacohen
| 期刊: | Nature Biotechnology | 影响因子: | 33.100 |
| 时间: | 2024 | 起止号: | 2024 Apr;42(4):582-586. |
| doi: | 10.1038/s41587-023-01815-7 | 研究方向: | 其它 |
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.
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