High-throughput RNA isoform sequencing using programmed cDNA concatenation

被引:0
|
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
机构
[1] Broad Institute of MIT and Harvard,Department of Medicine
[2] Center for Cancer Research,Department of Pediatrics
[3] Massachusetts General Hospital,Division of Hematology/Oncology
[4] Harvard Medical School,Department of Pediatric Oncology
[5] Boston Children’s Hospital,Division of Surgical Oncology
[6] Dana Farber Cancer Institute,Department of Biological Engineering
[7] Massachusetts General Hospital,Center for Immunology and Inflammatory Diseases
[8] Harvard Medical School,undefined
[9] Massachusetts Institute of Technology,undefined
[10] Koch Institute for Integrative Cancer Research at the Massachusetts Institute of Technology,undefined
[11] Harvard Medical School,undefined
[12] Massachusetts General Hospital,undefined
来源
Nature Biotechnology | 2024年 / 42卷
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摘要
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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页码:582 / 586
页数:4
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