» Articles » PMID: 32484809

RefShannon: A Genome-guided Transcriptome Assembler Using Sparse Flow Decomposition

Overview
Journal PLoS One
Date 2020 Jun 3
PMID 32484809
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

High throughput sequencing of RNA (RNA-Seq) has become a staple in modern molecular biology, with applications not only in quantifying gene expression but also in isoform-level analysis of the RNA transcripts. To enable such an isoform-level analysis, a transcriptome assembly algorithm is utilized to stitch together the observed short reads into the corresponding transcripts. This task is complicated due to the complexity of alternative splicing - a mechanism by which the same gene may generate multiple distinct RNA transcripts. We develop a novel genome-guided transcriptome assembler, RefShannon, that exploits the varying abundances of the different transcripts, in enabling an accurate reconstruction of the transcripts. Our evaluation shows RefShannon is able to improve sensitivity effectively (up to 22%) at a given specificity in comparison with other state-of-the-art assemblers. RefShannon is written in Python and is available from Github (https://github.com/shunfumao/RefShannon).

Citing Articles

Data-driven AI system for learning how to run transcript assemblers.

Shen Y, Yan Z, Kingsford C bioRxiv. 2024; .

PMID: 39554123 PMC: 11565938. DOI: 10.1101/2024.01.25.577290.


Induction of Invasive Basal Phenotype in Triple-Negative Breast Cancers by Long Noncoding RNA BORG.

Niazi F, Parker K, Mason S, Singh S, Schiemann W, Valadkhan S Cancers (Basel). 2024; 16(18).

PMID: 39335212 PMC: 11430157. DOI: 10.3390/cancers16183241.


ClusTrast: a short read de novo transcript isoform assembler guided by clustered contigs.

Westrin K, Kretzschmar W, Emanuelsson O BMC Bioinformatics. 2024; 25(1):54.

PMID: 38302873 PMC: 10836024. DOI: 10.1186/s12859-024-05663-3.


StringFix: an annotation-guided transcriptome assembler improves the recovery of amino acid sequences from RNA-Seq reads.

Lee J, Kim M, Han K, Yoon S Genes Genomics. 2023; 45(12):1599-1609.

PMID: 37837515 DOI: 10.1007/s13258-023-01458-7.


Accurate assembly of multi-end RNA-seq data with Scallop2.

Zhang Q, Shi Q, Shao M Nat Comput Sci. 2023; 2(3):148-152.

PMID: 36713932 PMC: 9879047. DOI: 10.1038/s43588-022-00216-1.


References
1.
Robertson G, Schein J, Chiu R, Corbett R, Field M, Jackman S . De novo assembly and analysis of RNA-seq data. Nat Methods. 2010; 7(11):909-12. DOI: 10.1038/nmeth.1517. View

2.
Au K, Sebastiano V, Afshar P, Durruthy J, Lee L, Williams B . Characterization of the human ESC transcriptome by hybrid sequencing. Proc Natl Acad Sci U S A. 2013; 110(50):E4821-30. PMC: 3864310. DOI: 10.1073/pnas.1320101110. View

3.
Trapnell C, Williams B, Pertea G, Mortazavi A, Kwan G, van Baren M . Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation. Nat Biotechnol. 2010; 28(5):511-5. PMC: 3146043. DOI: 10.1038/nbt.1621. View

4.
Steijger T, Abril J, Engstrom P, Kokocinski F, Hubbard T, Guigo R . Assessment of transcript reconstruction methods for RNA-seq. Nat Methods. 2013; 10(12):1177-84. PMC: 3851240. DOI: 10.1038/nmeth.2714. View

5.
Gilbert W . Why genes in pieces?. Nature. 1978; 271(5645):501. DOI: 10.1038/271501a0. View