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

阅读:3
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

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.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。