Cargando…

TrancriptomeReconstructoR: data-driven annotation of complex transcriptomes

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 shoul...

Descripción completa

Detalles Bibliográficos
Autores principales: Ivanov, Maxim, Sandelin, Albin, Marquardt, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166035/
https://www.ncbi.nlm.nih.gov/pubmed/34058980
http://dx.doi.org/10.1186/s12859-021-04208-2
_version_ 1783701434247675904
author Ivanov, Maxim
Sandelin, Albin
Marquardt, Sebastian
author_facet Ivanov, Maxim
Sandelin, Albin
Marquardt, Sebastian
author_sort Ivanov, Maxim
collection PubMed
description 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04208-2.
format Online
Article
Text
id pubmed-8166035
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-81660352021-06-02 TrancriptomeReconstructoR: data-driven annotation of complex transcriptomes Ivanov, Maxim Sandelin, Albin Marquardt, Sebastian BMC Bioinformatics Research 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04208-2. BioMed Central 2021-05-31 /pmc/articles/PMC8166035/ /pubmed/34058980 http://dx.doi.org/10.1186/s12859-021-04208-2 Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ivanov, Maxim
Sandelin, Albin
Marquardt, Sebastian
TrancriptomeReconstructoR: data-driven annotation of complex transcriptomes
title TrancriptomeReconstructoR: data-driven annotation of complex transcriptomes
title_full TrancriptomeReconstructoR: data-driven annotation of complex transcriptomes
title_fullStr TrancriptomeReconstructoR: data-driven annotation of complex transcriptomes
title_full_unstemmed TrancriptomeReconstructoR: data-driven annotation of complex transcriptomes
title_short TrancriptomeReconstructoR: data-driven annotation of complex transcriptomes
title_sort trancriptomereconstructor: data-driven annotation of complex transcriptomes
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8166035/
https://www.ncbi.nlm.nih.gov/pubmed/34058980
http://dx.doi.org/10.1186/s12859-021-04208-2
work_keys_str_mv AT ivanovmaxim trancriptomereconstructordatadrivenannotationofcomplextranscriptomes
AT sandelinalbin trancriptomereconstructordatadrivenannotationofcomplextranscriptomes
AT marquardtsebastian trancriptomereconstructordatadrivenannotationofcomplextranscriptomes