Sequencing of individual barcoded cDNAs using Pacific Biosciences and Oxford Nanopore Technologies reveals platform-specific error patterns
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Title
Sequencing of individual barcoded cDNAs using Pacific Biosciences and Oxford Nanopore Technologies reveals platform-specific error patterns
Authors
Keywords
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Journal
GENOME RESEARCH
Volume 32, Issue 4, Pages 726-737
Publisher
Cold Spring Harbor Laboratory
Online
2022-03-18
DOI
10.1101/gr.276405.121
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Note: Only part of the references are listed.- Single-nuclei isoform RNA sequencing unlocks barcoded exon connectivity in frozen brain tissue
- (2022) Simon A. Hardwick et al. NATURE BIOTECHNOLOGY
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- (2021) Anoushka Joglekar et al. Nature Communications
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- (2021) Kristoffer Sahlin et al. Nature Communications
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- (2021) Yu H. Sun et al. Nature Communications
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- (2021) Kristoffer Sahlin et al. BIOINFORMATICS
- Integrative analysis reveals RNA G-quadruplexes in UTRs are selectively constrained and enriched for functional associations
- (2020) David S. M. Lee et al. Nature Communications
- Full-length transcript characterization of SF3B1 mutation in chronic lymphocytic leukemia reveals downregulation of retained introns
- (2020) Alison D. Tang et al. Nature Communications
- Ultralow-input single-tube linked-read library method enables short-read second-generation sequencing systems to routinely generate highly accurate and economical long-range sequencing information
- (2020) Zhoutao Chen et al. GENOME RESEARCH
- Analysis and comprehensive comparison of PacBio and nanopore-based RNA sequencing of the Arabidopsis transcriptome
- (2020) Jiawen Cui et al. Plant Methods
- Trans-NanoSim characterizes and simulates nanopore RNA-sequencing data
- (2020) Saber Hafezqorani et al. GigaScience
- GENCODE 2021
- (2020) Adam Frankish et al. NUCLEIC ACIDS RESEARCH
- Direct RNA sequencing on nanopore arrays redefines the transcriptional complexity of a viral pathogen
- (2019) Daniel P. Depledge et al. Nature Communications
- Single-molecule long-read sequencing reveals the chromatin basis of gene expression
- (2019) Yunhao Wang et al. GENOME RESEARCH
- High-throughput targeted long-read single cell sequencing reveals the clonal and transcriptional landscape of lymphocytes
- (2019) Mandeep Singh et al. Nature Communications
- PolyASite 2.0: a consolidated atlas of polyadenylation sites from 3′ end sequencing
- (2019) Christina J Herrmann et al. NUCLEIC ACIDS RESEARCH
- Minimap2: pairwise alignment for nucleotide sequences
- (2018) Heng Li BIOINFORMATICS
- SQANTI: extensive characterization of long-read transcript sequences for quality control in full-length transcriptome identification and quantification
- (2018) Manuel Tardaguila et al. GENOME RESEARCH
- Highly parallel direct RNA sequencing on an array of nanopores
- (2018) Daniel R Garalde et al. NATURE METHODS
- Improving nanopore read accuracy with the R2C2 method enables the sequencing of highly multiplexed full-length single-cell cDNA
- (2018) Roger Volden et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Single-cell isoform RNA sequencing characterizes isoforms in thousands of cerebellar cells
- (2018) Ishaan Gupta et al. NATURE BIOTECHNOLOGY
- Microfluidic isoform sequencing shows widespread splicing coordination in the human transcriptome
- (2017) Hagen Tilgner et al. GENOME RESEARCH
- Nanopore long-read RNAseq reveals widespread transcriptional variation among the surface receptors of individual B cells
- (2017) Ashley Byrne et al. Nature Communications
- A new view of transcriptome complexity and regulation through the lens of local splicing variations
- (2016) Jorge Vaquero-Garcia et al. eLife
- Benchmarking of the Oxford Nanopore MinION sequencing for quantitative and qualitative assessment of cDNA populations
- (2016) Spyros Oikonomopoulos et al. Scientific Reports
- Highly Parallel Genome-wide Expression Profiling of Individual Cells Using Nanoliter Droplets
- (2015) Evan Z. Macosko et al. CELL
- Comprehensive transcriptome analysis using synthetic long-read sequencing reveals molecular co-association of distant splicing events
- (2015) Hagen Tilgner et al. NATURE BIOTECHNOLOGY
- Characterization of fusion genes and the significantly expressed fusion isoforms in breast cancer by hybrid sequencing
- (2015) Jason L. Weirather et al. NUCLEIC ACIDS RESEARCH
- Cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq
- (2015) A. Zeisel et al. SCIENCE
- Gateways to the FANTOM5 promoter level mammalian expression atlas
- (2015) Marina Lizio et al. GENOME BIOLOGY
- Multi-platform assessment of transcriptome profiling using RNA-seq in the ABRF next-generation sequencing study
- (2014) Sheng Li et al. NATURE BIOTECHNOLOGY
- Detecting and correcting systematic variation in large-scale RNA sequencing data
- (2014) Sheng Li et al. NATURE BIOTECHNOLOGY
- Defining a personal, allele-specific, and single-molecule long-read transcriptome
- (2014) Hagen Tilgner et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- A single-molecule long-read survey of the human transcriptome
- (2013) Donald Sharon et al. NATURE BIOTECHNOLOGY
- Assessment of transcript reconstruction methods for RNA-seq
- (2013) Tamara Steijger et al. NATURE METHODS
- Systematic evaluation of spliced alignment programs for RNA-seq data
- (2013) Pär G Engström et al. NATURE METHODS
- SSW Library: An SIMD Smith-Waterman C/C++ Library for Use in Genomic Applications
- (2013) Mengyao Zhao et al. PLoS One
- Characterization of the human ESC transcriptome by hybrid sequencing
- (2013) K. F. Au et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Accurate Identification and Analysis of Human mRNA Isoforms Using Deep Long Read Sequencing
- (2013) Hagen Tilgner et al. G3-Genes Genomes Genetics
- STAR: ultrafast universal RNA-seq aligner
- (2012) Alexander Dobin et al. BIOINFORMATICS
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- (2012) Sergey Koren et al. NATURE BIOTECHNOLOGY
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- (2012) Kin Fai Au et al. PLoS One
- Measurement of mRNA abundance using RNA-seq data: RPKM measure is inconsistent among samples
- (2012) Günter P. Wagner et al. THEORY IN BIOSCIENCES
- Computational prediction of Caenorhabditis box H/ACA snoRNAs using genomic properties of their host genes
- (2009) P. P.-S. Wang et al. RNA
- Alternative isoform regulation in human tissue transcriptomes
- (2008) Eric T. Wang et al. NATURE
- Real-Time DNA Sequencing from Single Polymerase Molecules
- (2008) J. Eid et al. SCIENCE
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