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CoCo: RNA-seq read assignment correction for nested genes and multimapped reads

MOTIVATION: Next-generation sequencing techniques revolutionized the study of RNA expression by permitting whole transcriptome analysis. However, sequencing reads generated from nested and multi-copy genes are often either misassigned or discarded, which greatly reduces both quantification accuracy...

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Detalles Bibliográficos
Autores principales: Deschamps-Francoeur, Gabrielle, Boivin, Vincent, Abou Elela, Sherif, Scott, Michelle S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6901076/
https://www.ncbi.nlm.nih.gov/pubmed/31141144
http://dx.doi.org/10.1093/bioinformatics/btz433
Descripción
Sumario:MOTIVATION: Next-generation sequencing techniques revolutionized the study of RNA expression by permitting whole transcriptome analysis. However, sequencing reads generated from nested and multi-copy genes are often either misassigned or discarded, which greatly reduces both quantification accuracy and gene coverage. RESULTS: Here we present count corrector (CoCo), a read assignment pipeline that takes into account the multitude of overlapping and repetitive genes in the transcriptome of higher eukaryotes. CoCo uses a modified annotation file that highlights nested genes and proportionally distributes multimapped reads between repeated sequences. CoCo salvages over 15% of discarded aligned RNA-seq reads and significantly changes the abundance estimates for both coding and non-coding RNA as validated by PCR and bedgraph comparisons. AVAILABILITY AND IMPLEMENTATION: The CoCo software is an open source package written in Python and available from http://gitlabscottgroup.med.usherbrooke.ca/scott-group/coco. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.