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RNA-Bloom enables reference-free and reference-guided sequence assembly for single-cell transcriptomes
Despite the rapid advance in single-cell RNA sequencing (scRNA-seq) technologies within the last decade, single-cell transcriptome analysis workflows have primarily used gene expression data while isoform sequence analysis at the single-cell level still remains fairly limited. Detection and discover...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462077/ https://www.ncbi.nlm.nih.gov/pubmed/32817073 http://dx.doi.org/10.1101/gr.260174.119 |
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author | Nip, Ka Ming Chiu, Readman Yang, Chen Chu, Justin Mohamadi, Hamid Warren, René L. Birol, Inanc |
author_facet | Nip, Ka Ming Chiu, Readman Yang, Chen Chu, Justin Mohamadi, Hamid Warren, René L. Birol, Inanc |
author_sort | Nip, Ka Ming |
collection | PubMed |
description | Despite the rapid advance in single-cell RNA sequencing (scRNA-seq) technologies within the last decade, single-cell transcriptome analysis workflows have primarily used gene expression data while isoform sequence analysis at the single-cell level still remains fairly limited. Detection and discovery of isoforms in single cells is difficult because of the inherent technical shortcomings of scRNA-seq data, and existing transcriptome assembly methods are mainly designed for bulk RNA samples. To address this challenge, we developed RNA-Bloom, an assembly algorithm that leverages the rich information content aggregated from multiple single-cell transcriptomes to reconstruct cell-specific isoforms. Assembly with RNA-Bloom can be either reference-guided or reference-free, thus enabling unbiased discovery of novel isoforms or foreign transcripts. We compared both assembly strategies of RNA-Bloom against five state-of-the-art reference-free and reference-based transcriptome assembly methods. In our benchmarks on a simulated 384-cell data set, reference-free RNA-Bloom reconstructed 37.9%–38.3% more isoforms than the best reference-free assembler, whereas reference-guided RNA-Bloom reconstructed 4.1%–11.6% more isoforms than reference-based assemblers. When applied to a real 3840-cell data set consisting of more than 4 billion reads, RNA-Bloom reconstructed 9.7%–25.0% more isoforms than the best competing reference-based and reference-free approaches evaluated. We expect RNA-Bloom to boost the utility of scRNA-seq data beyond gene expression analysis, expanding what is informatically accessible now. |
format | Online Article Text |
id | pubmed-7462077 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-74620772020-09-11 RNA-Bloom enables reference-free and reference-guided sequence assembly for single-cell transcriptomes Nip, Ka Ming Chiu, Readman Yang, Chen Chu, Justin Mohamadi, Hamid Warren, René L. Birol, Inanc Genome Res Method Despite the rapid advance in single-cell RNA sequencing (scRNA-seq) technologies within the last decade, single-cell transcriptome analysis workflows have primarily used gene expression data while isoform sequence analysis at the single-cell level still remains fairly limited. Detection and discovery of isoforms in single cells is difficult because of the inherent technical shortcomings of scRNA-seq data, and existing transcriptome assembly methods are mainly designed for bulk RNA samples. To address this challenge, we developed RNA-Bloom, an assembly algorithm that leverages the rich information content aggregated from multiple single-cell transcriptomes to reconstruct cell-specific isoforms. Assembly with RNA-Bloom can be either reference-guided or reference-free, thus enabling unbiased discovery of novel isoforms or foreign transcripts. We compared both assembly strategies of RNA-Bloom against five state-of-the-art reference-free and reference-based transcriptome assembly methods. In our benchmarks on a simulated 384-cell data set, reference-free RNA-Bloom reconstructed 37.9%–38.3% more isoforms than the best reference-free assembler, whereas reference-guided RNA-Bloom reconstructed 4.1%–11.6% more isoforms than reference-based assemblers. When applied to a real 3840-cell data set consisting of more than 4 billion reads, RNA-Bloom reconstructed 9.7%–25.0% more isoforms than the best competing reference-based and reference-free approaches evaluated. We expect RNA-Bloom to boost the utility of scRNA-seq data beyond gene expression analysis, expanding what is informatically accessible now. Cold Spring Harbor Laboratory Press 2020-08 /pmc/articles/PMC7462077/ /pubmed/32817073 http://dx.doi.org/10.1101/gr.260174.119 Text en © 2020 Nip et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Method Nip, Ka Ming Chiu, Readman Yang, Chen Chu, Justin Mohamadi, Hamid Warren, René L. Birol, Inanc RNA-Bloom enables reference-free and reference-guided sequence assembly for single-cell transcriptomes |
title | RNA-Bloom enables reference-free and reference-guided sequence assembly for single-cell transcriptomes |
title_full | RNA-Bloom enables reference-free and reference-guided sequence assembly for single-cell transcriptomes |
title_fullStr | RNA-Bloom enables reference-free and reference-guided sequence assembly for single-cell transcriptomes |
title_full_unstemmed | RNA-Bloom enables reference-free and reference-guided sequence assembly for single-cell transcriptomes |
title_short | RNA-Bloom enables reference-free and reference-guided sequence assembly for single-cell transcriptomes |
title_sort | rna-bloom enables reference-free and reference-guided sequence assembly for single-cell transcriptomes |
topic | Method |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462077/ https://www.ncbi.nlm.nih.gov/pubmed/32817073 http://dx.doi.org/10.1101/gr.260174.119 |
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