F1000ResearchBioinformaticsPeer-reviewed journal article
Scavenger: A pipeline for recovery of unaligned reads utilising similarity with aligned reads
Andrian YangiD, Joshua Y. S. Tang, Michael TroupiD, Joshua W. K. HoiD
Abstract
MotivationRead alignment is an important step in RNA-seq analysis as the result of alignment forms the basis for further downstream analyses. However, recent studies have shown that published alignment tools have variable mapping sensitivity and do not necessarily align reads which should have been aligned, a problem we termed as the false-negative non-alignment problem.\n\nResultsWe have developed Scavenger, a pipeline for recovering unaligned reads using a novel mechanism which utilises information from aligned reads. Scavenger performs recovery of unaligned reads by re-aligning unaligned reads against a putative location derived from aligned reads with sequence similarity against unaligned reads. We show that Scavenger can successfully recover unaligned reads in both simulated and real RNA-seq datasets, including single-cell RNA-seq data. The reads recovered contain more genetic variants compared to previously aligned reads, indicating that divergence between personal and reference genomes plays a role in the false-negative non-alignment problem. We also explored the impact of read recovery on downstream analyses, in particular gene expression analysis, and showed that Scavenger is able to both recover genes which were previously non-expressed and also increase gene expression, with lowly expressed genes having the most impact from the addition of recovered reads. We also found that the majority of genes with >1 fold change in expression after recovery are categorised as pseudogenes, indicating that pseudogene expression can be affected by the false-negative non-alignment problem. Scavenger helps to solve the false-negative non-alignment problem through recovery of unaligned reads using information from previously aligned reads.\n\nAvailabilityScavenger is available via an open source license in https://github.com/VCCRI/Scavenger/\n\nContactj.ho@victorchang.edu.au
- assay: bulk RNA-seq
- assay: scRNA-seq
- research focus: differential expression
- research focus: benchmarking
- research focus: gene regulatory network inference
- approach: statistical model
- Citations
- 2
- FWCI
- 0.08
- Field percentile
- 39th percentile
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Shark: fishing in a sample to discard useless RNA-Seq reads
Luca Denti, Yuri Pirola, … Paola Bonizzoni·BioinformaticsPeer-reviewed·Sep 2, 2020
- STAR: ultrafast universal RNA-seq aligner
Alexander Dobin, Carrie Davis, … T Gingeras·BioinformaticsPeer-reviewed·Oct 25, 2012
- Evaluation of tools for long read RNA-seq splice-aware alignment
Krešimir Križanović, Amina Echchiki, … Mile Šikić·BioinformaticsPeer-reviewed·Oct 18, 2017
- The fractured landscape of RNA-seq alignment: The default in our STARs
Sara Ballouz, Alexander Dobin, … Jesse A Gillis·Nucleic Acids ResearchPeer-reviewed·Apr 16, 2018
- Detection and Mitigation of Spurious Antisense RNA-seq Reads with RoSA
Kira Mourão, Nicholas J. Schurch, … Geoffrey J. Barton·bioRxiv·Sep 26, 2018
- Towards selective-alignment: Bridging the accuracy gap between alignment-based and alignment-free transcript quantification
Hirak Sarkar, Mohsen Zakeri, … Rob Patro·bioRxiv·Aug 24, 2017