Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Department of Medicine, Center for Cancer Research, Massachusetts General Hospital, Boston, MA, USA.
Nat Biotechnol. 2024 Apr;42(4):582-586. doi: 10.1038/s41587-023-01815-7. Epub 2023 Jun 8.
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.
全长 RNA 测序方法结合长读长技术可以捕获完整的转录本异构体,但通量有限。我们介绍了多重阵列异构体测序 (MAS-ISO-seq),这是一种将互补 DNA (cDNA) 编程连接成最适合长读长测序的分子的技术,在 Sequel IIe 测序仪上的每个运行中,通量增加了 >15 倍,达到近 4000 万 cDNA 读长。当应用于肿瘤浸润 T 细胞的单细胞 RNA 测序时,MAS-ISO-seq 显示差异剪接基因的发现增加了 12 到 32 倍。