SRSF shape analysis for sequencing data reveal newdifferentiating patterns
Abstract
MotivationSequencing-based methods to examine fundamental features of the genome, such as gene expression and chromatin structure, rely on inferences from the abundance and distribution of reads derived from Illumina sequencing. Drawing sound inferences from such experiments relies on appropriate mathematical methods to model the distribution of reads along the genome, which has been challenging due to the scale and nature of these data.\n\nResultsWe propose a new framework (SRSFseq) based on Square Root Slope Functions shape analysis to analyse Illumina sequencing data. In the new approach the basic unit of information is the density of mapped reads over region of interest located on the known reference genome. The densities are interpreted as shapes and a new shape analysis model is proposed. An equivalent of a Fisher test is used to quantify the significance of shape differences in read distribution patterns between groups of density functions in different experimental conditions. We evaluated the performance of this new framework to analyze RNA-seq data at the exon level, which enabled the detection of variation in read distributions and abundances between experimental conditions not detected by other methods. Thus, the method is a suitable supplement to the state of the are count based techniques. The variety of density representations and flexibility of mathematical design allow the model to be easily adapted to other data types or problems in which the distribution of reads is to be tested. The functional interpretation and SRSF phase-amplitude separation technique gives an efficient noise reduction procedure improving the sensitivity and specificity of the method.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 2
- FWCI
- 0.11
- Field percentile
- 48th percentile
- Assay
- Research Focus
- Approach
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
- The R package Rsubread is easier, faster, cheaper and better for alignment and quantification of RNA sequencing reads
Yang Liao, Gordon K. Smyth, Wei Shi·Nucleic Acids ResearchPeer-reviewed·Feb 17, 2019
- Sashimi plots: Quantitative visualization of alternative isoform expression from RNA-seq data
Yarden Katz, Eric T Wang, … Christopher B Burge·BioinformaticsPeer-reviewed·Jan 22, 2015
- q-mer analysis: a generalized method for analyzing RNA-Seq data.
Tatsuma Shoji, Yoshiharu Sato·bioRxiv·May 1, 2021
- Making sense of RNA-Seq data: from low-level processing to functional analysis
Oleg V. Moskvin, Sean McIlwain, Irene M. Ong·bioRxiv·Oct 17, 2014
- Nonparametric expression analysis using inferential replicate counts
Anqi Zhu, Avi Srivastava, … Michael I. Love·Nucleic Acids ResearchPeer-reviewed·Jul 11, 2019
- VERSE: a versatile and efficient RNA-Seq read counting tool
Qin Zhu, Stephen A Fisher, … Junhyong Kim·bioRxiv·May 14, 2016