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Comparability of reference-based and reference-free transcriptome analysis approaches at the gene expression level
BACKGROUND: Lately, high-throughput RNA sequencing has been extensively used to elucidate the transcriptome landscape and dynamics of cell types of different species. In particular, for most non-model organisms lacking complete reference genomes with high-quality annotation of genetic information, r...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529712/ https://www.ncbi.nlm.nih.gov/pubmed/34674628 http://dx.doi.org/10.1186/s12859-021-04226-0 |
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author | Lee, Sung-Gwon Na, Dokyun Park, Chungoo |
author_facet | Lee, Sung-Gwon Na, Dokyun Park, Chungoo |
author_sort | Lee, Sung-Gwon |
collection | PubMed |
description | BACKGROUND: Lately, high-throughput RNA sequencing has been extensively used to elucidate the transcriptome landscape and dynamics of cell types of different species. In particular, for most non-model organisms lacking complete reference genomes with high-quality annotation of genetic information, reference-free (RF) de novo transcriptome analyses, rather than reference-based (RB) approaches, are widely used, and RF analyses have substantially contributed toward understanding the mechanisms regulating key biological processes and functions. To date, numerous bioinformatics studies have been conducted for assessing the workflow, production rate, and completeness of transcriptome assemblies within and between RF and RB datasets. However, the degree of consistency and variability of results obtained by analyzing gene expression levels through these two different approaches have not been adequately documented. RESULTS: In the present study, we evaluated the differences in expression profiles obtained with RF and RB approaches and revealed that the former tends to be satisfactorily replaced by the latter with respect to transcriptome repertoires, as well as from a gene expression quantification perspective. In addition, we urge cautious interpretation of these findings. Several genes that are lowly expressed, have long coding sequences, or belong to large gene families must be validated carefully, whenever gene expression levels are calculated using the RF method. CONCLUSIONS: Our empirical results indicate important contributions toward addressing transcriptome-related biological questions in non-model organisms. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04226-0. |
format | Online Article Text |
id | pubmed-8529712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85297122021-10-25 Comparability of reference-based and reference-free transcriptome analysis approaches at the gene expression level Lee, Sung-Gwon Na, Dokyun Park, Chungoo BMC Bioinformatics Research BACKGROUND: Lately, high-throughput RNA sequencing has been extensively used to elucidate the transcriptome landscape and dynamics of cell types of different species. In particular, for most non-model organisms lacking complete reference genomes with high-quality annotation of genetic information, reference-free (RF) de novo transcriptome analyses, rather than reference-based (RB) approaches, are widely used, and RF analyses have substantially contributed toward understanding the mechanisms regulating key biological processes and functions. To date, numerous bioinformatics studies have been conducted for assessing the workflow, production rate, and completeness of transcriptome assemblies within and between RF and RB datasets. However, the degree of consistency and variability of results obtained by analyzing gene expression levels through these two different approaches have not been adequately documented. RESULTS: In the present study, we evaluated the differences in expression profiles obtained with RF and RB approaches and revealed that the former tends to be satisfactorily replaced by the latter with respect to transcriptome repertoires, as well as from a gene expression quantification perspective. In addition, we urge cautious interpretation of these findings. Several genes that are lowly expressed, have long coding sequences, or belong to large gene families must be validated carefully, whenever gene expression levels are calculated using the RF method. CONCLUSIONS: Our empirical results indicate important contributions toward addressing transcriptome-related biological questions in non-model organisms. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-021-04226-0. BioMed Central 2021-10-21 /pmc/articles/PMC8529712/ /pubmed/34674628 http://dx.doi.org/10.1186/s12859-021-04226-0 Text en © The Author(s) 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 Lee, Sung-Gwon Na, Dokyun Park, Chungoo Comparability of reference-based and reference-free transcriptome analysis approaches at the gene expression level |
title | Comparability of reference-based and reference-free transcriptome analysis approaches at the gene expression level |
title_full | Comparability of reference-based and reference-free transcriptome analysis approaches at the gene expression level |
title_fullStr | Comparability of reference-based and reference-free transcriptome analysis approaches at the gene expression level |
title_full_unstemmed | Comparability of reference-based and reference-free transcriptome analysis approaches at the gene expression level |
title_short | Comparability of reference-based and reference-free transcriptome analysis approaches at the gene expression level |
title_sort | comparability of reference-based and reference-free transcriptome analysis approaches at the gene expression level |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529712/ https://www.ncbi.nlm.nih.gov/pubmed/34674628 http://dx.doi.org/10.1186/s12859-021-04226-0 |
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