TrancriptomeReconstructoR: data-driven annotation of complex transcriptomes

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TrancriptomeReconstructoR : data-driven annotation of complex transcriptomes. / Ivanov, Maxim; Sandelin, Albin; Marquardt, Sebastian.

In: BMC Bioinformatics, Vol. 22, 290, 2021.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Ivanov, M, Sandelin, A & Marquardt, S 2021, 'TrancriptomeReconstructoR: data-driven annotation of complex transcriptomes', BMC Bioinformatics, vol. 22, 290. https://doi.org/10.1186/s12859-021-04208-2

APA

Ivanov, M., Sandelin, A., & Marquardt, S. (2021). TrancriptomeReconstructoR: data-driven annotation of complex transcriptomes. BMC Bioinformatics, 22, [290]. https://doi.org/10.1186/s12859-021-04208-2

Vancouver

Ivanov M, Sandelin A, Marquardt S. TrancriptomeReconstructoR: data-driven annotation of complex transcriptomes. BMC Bioinformatics. 2021;22. 290. https://doi.org/10.1186/s12859-021-04208-2

Author

Ivanov, Maxim ; Sandelin, Albin ; Marquardt, Sebastian. / TrancriptomeReconstructoR : data-driven annotation of complex transcriptomes. In: BMC Bioinformatics. 2021 ; Vol. 22.

Bibtex

@article{35da6c7f0edd4de3928ec0cf50abd9f1,
title = "TrancriptomeReconstructoR: data-driven annotation of complex transcriptomes",
abstract = "Background: The quality of gene annotation determines the interpretation of results obtained in transcriptomic studies. The growing number of genome sequence information calls for experimental and computational pipelines for de novo transcriptome annotation. Ideally, gene and transcript models should be called from a limited set of key experimental data. Results: We developed TranscriptomeReconstructoR, an R package which implements a pipeline for automated transcriptome annotation. It relies on integrating features from independent and complementary datasets: (i) full-length RNA-seq for detection of splicing patterns and (ii) high-throughput 5′ and 3′ tag sequencing data for accurate definition of gene borders. The pipeline can also take a nascent RNA-seq dataset to supplement the called gene model with transient transcripts. We reconstructed de novo the transcriptional landscape of wild type Arabidopsis thaliana seedlings and Saccharomyces cerevisiae cells as a proof-of-principle. A comparison to the existing transcriptome annotations revealed that our gene model is more accurate and comprehensive than the most commonly used community gene models, TAIR10 and Araport11 for A.thaliana and SacCer3 for S.cerevisiae. In particular, we identify multiple transient transcripts missing from the existing annotations. Our new annotations promise to improve the quality of A.thaliana and S.cerevisiae genome research. Conclusions: Our proof-of-concept data suggest a cost-efficient strategy for rapid and accurate annotation of complex eukaryotic transcriptomes. We combine the choice of library preparation methods and sequencing platforms with the dedicated computational pipeline implemented in the TranscriptomeReconstructoR package. The pipeline only requires prior knowledge on the reference genomic DNA sequence, but not the transcriptome. The package seamlessly integrates with Bioconductor packages for downstream analysis.",
author = "Maxim Ivanov and Albin Sandelin and Sebastian Marquardt",
note = "Publisher Copyright: {\textcopyright} 2021, The Author(s).",
year = "2021",
doi = "10.1186/s12859-021-04208-2",
language = "English",
volume = "22",
journal = "B M C Bioinformatics",
issn = "1471-2105",
publisher = "BioMed Central Ltd.",

}

RIS

TY - JOUR

T1 - TrancriptomeReconstructoR

T2 - data-driven annotation of complex transcriptomes

AU - Ivanov, Maxim

AU - Sandelin, Albin

AU - Marquardt, Sebastian

N1 - Publisher Copyright: © 2021, The Author(s).

PY - 2021

Y1 - 2021

N2 - Background: The quality of gene annotation determines the interpretation of results obtained in transcriptomic studies. The growing number of genome sequence information calls for experimental and computational pipelines for de novo transcriptome annotation. Ideally, gene and transcript models should be called from a limited set of key experimental data. Results: We developed TranscriptomeReconstructoR, an R package which implements a pipeline for automated transcriptome annotation. It relies on integrating features from independent and complementary datasets: (i) full-length RNA-seq for detection of splicing patterns and (ii) high-throughput 5′ and 3′ tag sequencing data for accurate definition of gene borders. The pipeline can also take a nascent RNA-seq dataset to supplement the called gene model with transient transcripts. We reconstructed de novo the transcriptional landscape of wild type Arabidopsis thaliana seedlings and Saccharomyces cerevisiae cells as a proof-of-principle. A comparison to the existing transcriptome annotations revealed that our gene model is more accurate and comprehensive than the most commonly used community gene models, TAIR10 and Araport11 for A.thaliana and SacCer3 for S.cerevisiae. In particular, we identify multiple transient transcripts missing from the existing annotations. Our new annotations promise to improve the quality of A.thaliana and S.cerevisiae genome research. Conclusions: Our proof-of-concept data suggest a cost-efficient strategy for rapid and accurate annotation of complex eukaryotic transcriptomes. We combine the choice of library preparation methods and sequencing platforms with the dedicated computational pipeline implemented in the TranscriptomeReconstructoR package. The pipeline only requires prior knowledge on the reference genomic DNA sequence, but not the transcriptome. The package seamlessly integrates with Bioconductor packages for downstream analysis.

AB - Background: The quality of gene annotation determines the interpretation of results obtained in transcriptomic studies. The growing number of genome sequence information calls for experimental and computational pipelines for de novo transcriptome annotation. Ideally, gene and transcript models should be called from a limited set of key experimental data. Results: We developed TranscriptomeReconstructoR, an R package which implements a pipeline for automated transcriptome annotation. It relies on integrating features from independent and complementary datasets: (i) full-length RNA-seq for detection of splicing patterns and (ii) high-throughput 5′ and 3′ tag sequencing data for accurate definition of gene borders. The pipeline can also take a nascent RNA-seq dataset to supplement the called gene model with transient transcripts. We reconstructed de novo the transcriptional landscape of wild type Arabidopsis thaliana seedlings and Saccharomyces cerevisiae cells as a proof-of-principle. A comparison to the existing transcriptome annotations revealed that our gene model is more accurate and comprehensive than the most commonly used community gene models, TAIR10 and Araport11 for A.thaliana and SacCer3 for S.cerevisiae. In particular, we identify multiple transient transcripts missing from the existing annotations. Our new annotations promise to improve the quality of A.thaliana and S.cerevisiae genome research. Conclusions: Our proof-of-concept data suggest a cost-efficient strategy for rapid and accurate annotation of complex eukaryotic transcriptomes. We combine the choice of library preparation methods and sequencing platforms with the dedicated computational pipeline implemented in the TranscriptomeReconstructoR package. The pipeline only requires prior knowledge on the reference genomic DNA sequence, but not the transcriptome. The package seamlessly integrates with Bioconductor packages for downstream analysis.

U2 - 10.1186/s12859-021-04208-2

DO - 10.1186/s12859-021-04208-2

M3 - Journal article

C2 - 34058980

AN - SCOPUS:85107323749

VL - 22

JO - B M C Bioinformatics

JF - B M C Bioinformatics

SN - 1471-2105

M1 - 290

ER -

ID: 273018853