ArticleBioinformatics (Oxford, England)2014
RNA-Skim: a rapid method for RNA-Seq quantification at transcript level.
Article in Bioinformatics (Oxford, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.
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23 citing papers in PubMed, 55 citations in OpenAlex.
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- Alignment and mapping methodology influence transcript abundance estimation.Genome biology · 2020Article
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- Matataki: an ultrafast mRNA quantification method for large-scale reanalysis of RNA-Seq data.BMC bioinformatics · 2018Article
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- Alignment-free sequence comparison: benefits, applications, and tools.Genome biology · 2017Review
- Integration of quantitated expression estimates from polyA-selected and rRNA-depleted RNA-seq libraries.BMC bioinformatics · 2017Article
- RapMap: a rapid, sensitive and accurate tool for mapping RNA-seq reads to transcriptomes.Bioinformatics (Oxford, England) · 2016Article
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2 authors at 1 institution in 1 country.
Funding
Abstract
motivationRNA-Seq technique has been demonstrated as a revolutionary means for exploring transcriptome because it provides deep coverage and base pair-level resolution. RNA-Seq quantification is proven to be an efficient alternative to Microarray technique in gene expression study, and it is a critical component in RNA-Seq differential expression analysis. Most existing RNA-Seq quantification tools require the alignments of fragments to either a genome or a transcriptome, entailing a time-consuming and intricate alignment step. To improve the performance of RNA-Seq quantification, an alignment-free method, Sailfish, has been recently proposed to quantify transcript abundances using all k-mers in the transcriptome, demonstrating the feasibility of designing an efficient alignment-free method for transcriptome quantification. Even though Sailfish is substantially faster than alternative alignment-dependent methods such as Cufflinks, using all k-mers in the transcriptome quantification impedes the scalability of the method.
resultsWe propose a novel RNA-Seq quantification method, RNA-Skim, which partitions the transcriptome into disjoint transcript clusters based on sequence similarity, and introduces the notion of sig-mers, which are a special type of k-mers uniquely associated with each cluster. We demonstrate that the sig-mer counts within a cluster are sufficient for estimating transcript abundances with accuracy comparable with any state-of-the-art method. This enables RNA-Skim to perform transcript quantification on each cluster independently, reducing a complex optimization problem into smaller optimization tasks that can be run in parallel. As a result, RNA-Skim uses <4% of the k-mers and <10% of the CPU time required by Sailfish. It is able to finish transcriptome quantification in <10 min per sample by using just a single thread on a commodity computer, which represents >100 speedup over the state-of-the-art alignment-based methods, while delivering comparable or higher accuracy. AVAILABILITY AND IMPLEMENTATION: The software is available at http://www.csbio.unc.edu/rs.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.