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使用可编程 cDNA 连接的高通量 RNA 异构体测序。

High-throughput RNA isoform sequencing using programmed cDNA concatenation.

机构信息

Broad Institute of MIT and Harvard, Cambridge, MA, USA.

Department of Medicine, Center for Cancer Research, Massachusetts General Hospital, Boston, MA, USA.

出版信息

Nat Biotechnol. 2024 Apr;42(4):582-586. doi: 10.1038/s41587-023-01815-7. Epub 2023 Jun 8.

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.

摘要

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。

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