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Single-cell long-read targeted sequencing reveals transcriptional variation in ovarian cancer
by
Byrne, Ashley
, Modrusan, Zora
, Sereti, Kostianna
, Shi, Minyi
, Menon, Hari
, Patel, Neha
, Vaidya, Samir
, Le, Daniel
, Xavier-Magalhães, Ana
, Sterne-Weiler, Timothy
, Liang, Yuxin
, Stephenson, William
, Lund, Jessica
in
13/62
/ 38/91
/ 45/41
/ 631/1647/2217/2018
/ 631/61/212/2019
/ 631/67/1517/1709
/ 631/67/69
/ Allelic Imbalance - genetics
/ Cancer
/ Cell Line, Tumor
/ Female
/ Gene Expression Profiling - methods
/ Gene Expression Regulation, Neoplastic
/ Gene sequencing
/ High-Throughput Nucleotide Sequencing - methods
/ Humanities and Social Sciences
/ Humans
/ Hybridization
/ Isoforms
/ multidisciplinary
/ Nucleotides
/ Ovarian cancer
/ Ovarian Neoplasms - genetics
/ Polymorphism, Single Nucleotide
/ Ribonucleic acid
/ RNA
/ RNA Isoforms - genetics
/ Science
/ Science (multidisciplinary)
/ Sequence Analysis, RNA - methods
/ Single-Cell Analysis - methods
/ Transcriptome - genetics
/ Transcriptomes
/ Tumor cell lines
2024
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Single-cell long-read targeted sequencing reveals transcriptional variation in ovarian cancer
by
Byrne, Ashley
, Modrusan, Zora
, Sereti, Kostianna
, Shi, Minyi
, Menon, Hari
, Patel, Neha
, Vaidya, Samir
, Le, Daniel
, Xavier-Magalhães, Ana
, Sterne-Weiler, Timothy
, Liang, Yuxin
, Stephenson, William
, Lund, Jessica
in
13/62
/ 38/91
/ 45/41
/ 631/1647/2217/2018
/ 631/61/212/2019
/ 631/67/1517/1709
/ 631/67/69
/ Allelic Imbalance - genetics
/ Cancer
/ Cell Line, Tumor
/ Female
/ Gene Expression Profiling - methods
/ Gene Expression Regulation, Neoplastic
/ Gene sequencing
/ High-Throughput Nucleotide Sequencing - methods
/ Humanities and Social Sciences
/ Humans
/ Hybridization
/ Isoforms
/ multidisciplinary
/ Nucleotides
/ Ovarian cancer
/ Ovarian Neoplasms - genetics
/ Polymorphism, Single Nucleotide
/ Ribonucleic acid
/ RNA
/ RNA Isoforms - genetics
/ Science
/ Science (multidisciplinary)
/ Sequence Analysis, RNA - methods
/ Single-Cell Analysis - methods
/ Transcriptome - genetics
/ Transcriptomes
/ Tumor cell lines
2024
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Single-cell long-read targeted sequencing reveals transcriptional variation in ovarian cancer
by
Byrne, Ashley
, Modrusan, Zora
, Sereti, Kostianna
, Shi, Minyi
, Menon, Hari
, Patel, Neha
, Vaidya, Samir
, Le, Daniel
, Xavier-Magalhães, Ana
, Sterne-Weiler, Timothy
, Liang, Yuxin
, Stephenson, William
, Lund, Jessica
in
13/62
/ 38/91
/ 45/41
/ 631/1647/2217/2018
/ 631/61/212/2019
/ 631/67/1517/1709
/ 631/67/69
/ Allelic Imbalance - genetics
/ Cancer
/ Cell Line, Tumor
/ Female
/ Gene Expression Profiling - methods
/ Gene Expression Regulation, Neoplastic
/ Gene sequencing
/ High-Throughput Nucleotide Sequencing - methods
/ Humanities and Social Sciences
/ Humans
/ Hybridization
/ Isoforms
/ multidisciplinary
/ Nucleotides
/ Ovarian cancer
/ Ovarian Neoplasms - genetics
/ Polymorphism, Single Nucleotide
/ Ribonucleic acid
/ RNA
/ RNA Isoforms - genetics
/ Science
/ Science (multidisciplinary)
/ Sequence Analysis, RNA - methods
/ Single-Cell Analysis - methods
/ Transcriptome - genetics
/ Transcriptomes
/ Tumor cell lines
2024
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Single-cell long-read targeted sequencing reveals transcriptional variation in ovarian cancer
Journal Article
Single-cell long-read targeted sequencing reveals transcriptional variation in ovarian cancer
2024
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Overview
Single-cell RNA sequencing predominantly employs short-read sequencing to characterize cell types, states and dynamics; however, it is inadequate for comprehensive characterization of RNA isoforms. Long-read sequencing technologies enable single-cell RNA isoform detection but are hampered by lower throughput and unintended sequencing of artifacts. Here we develop Single-cell Targeted Isoform Long-Read Sequencing (scTaILoR-seq), a hybridization capture method which targets over a thousand genes of interest, improving the median number of on-target transcripts per cell by 29-fold. We use scTaILoR-seq to identify and quantify RNA isoforms from ovarian cancer cell lines and primary tumors, yielding 10,796 single-cell transcriptomes. Using long-read variant calling we reveal associations of expressed single nucleotide variants (SNVs) with alternative transcript structures. Phasing of SNVs across transcripts enables the measurement of allelic imbalance within distinct cell populations. Overall, scTaILoR-seq is a long-read targeted RNA sequencing method and analytical framework for exploring transcriptional variation at single-cell resolution.
Long-read sequencing allows the detection of RNA isoforms, but is hampered by low throughput and potential artefacts. Here, the authors develop the scTaILoR-seq hybridisation capture method for long-read RNA sequencing to improve transcript detection, and use this method to detect isoforms at the single-cell level in ovarian cancer.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ 38/91
/ 45/41
/ Allelic Imbalance - genetics
/ Cancer
/ Female
/ Gene Expression Profiling - methods
/ Gene Expression Regulation, Neoplastic
/ High-Throughput Nucleotide Sequencing - methods
/ Humanities and Social Sciences
/ Humans
/ Isoforms
/ Ovarian Neoplasms - genetics
/ Polymorphism, Single Nucleotide
/ RNA
/ Science
/ Sequence Analysis, RNA - methods
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