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Article: BRIE: Transcriptome-wide splicing quantification in single cells

TitleBRIE: Transcriptome-wide splicing quantification in single cells
Authors
KeywordsIsoform estimate
Differential splicing
Single-cell RNA-seq
Issue Date2017
Citation
Genome Biology, 2017, v. 18, n. 1, article no. 123 How to Cite?
Abstract© 2017 The Author(s). Single-cell RNA-seq (scRNA-seq) provides a comprehensive measurement of stochasticity in transcription, but the limitations of the technology have prevented its application to dissect variability in RNA processing events such as splicing. Here, we present BRIE (Bayesian regression for isoform estimation), a Bayesian hierarchical model that resolves these problems by learning an informative prior distribution from sequence features. We show that BRIE yields reproducible estimates of exon inclusion ratios in single cells and provides an effective tool for differential isoform quantification between scRNA-seq data sets. BRIE, therefore, expands the scope of scRNA-seq experiments to probe the stochasticity of RNA processing.
Persistent Identifierhttp://hdl.handle.net/10722/280631
ISSN
2012 Impact Factor: 10.288
2023 SCImago Journal Rankings: 7.197
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHuang, Yuanhua-
dc.contributor.authorSanguinetti, Guido-
dc.date.accessioned2020-02-17T14:34:31Z-
dc.date.available2020-02-17T14:34:31Z-
dc.date.issued2017-
dc.identifier.citationGenome Biology, 2017, v. 18, n. 1, article no. 123-
dc.identifier.issn1474-7596-
dc.identifier.urihttp://hdl.handle.net/10722/280631-
dc.description.abstract© 2017 The Author(s). Single-cell RNA-seq (scRNA-seq) provides a comprehensive measurement of stochasticity in transcription, but the limitations of the technology have prevented its application to dissect variability in RNA processing events such as splicing. Here, we present BRIE (Bayesian regression for isoform estimation), a Bayesian hierarchical model that resolves these problems by learning an informative prior distribution from sequence features. We show that BRIE yields reproducible estimates of exon inclusion ratios in single cells and provides an effective tool for differential isoform quantification between scRNA-seq data sets. BRIE, therefore, expands the scope of scRNA-seq experiments to probe the stochasticity of RNA processing.-
dc.languageeng-
dc.relation.ispartofGenome Biology-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectIsoform estimate-
dc.subjectDifferential splicing-
dc.subjectSingle-cell RNA-seq-
dc.titleBRIE: Transcriptome-wide splicing quantification in single cells-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1186/s13059-017-1248-5-
dc.identifier.pmid28655331-
dc.identifier.pmcidPMC5488362-
dc.identifier.scopuseid_2-s2.0-85021264008-
dc.identifier.volume18-
dc.identifier.issue1-
dc.identifier.spagearticle no. 123-
dc.identifier.epagearticle no. 123-
dc.identifier.eissn1474-760X-
dc.identifier.isiWOS:000404154500001-
dc.identifier.issnl1474-7596-

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