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 40âmillion 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.
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:Al'Khafaji Aziz M, Smith Jonathan T, Garimella Kiran V, Babadi Mehrtash, Popic Victoria, Sade-Feldman Moshe, Gatzen Michael, Sarkizova Siranush, Schwartz Marc A, Blaum Emily M, Day Allyson, Costello Maura, Bowers Tera, Gabriel Stacey, Banks Eric, Philippakis Anthony A, Boland Genevieve M, Blainey Paul C, Hacohen Nir
| 期刊: | Nature Biotechnology | 影响因子: | 41.700 |
| 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 |
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