RNA-SeQC

RNA-SeQC assesses RNA sequencing (RNA-seq) data quality by computing metrics that evaluate sequencing performance and library quality for transcriptome analysis using next-generation sequencing.


Key Features:

  • Quality Control Metrics: Computes a suite of metrics including yield, alignment and duplication rates, GC bias, rRNA content, exon/intron/intragenic alignment distribution, coverage continuity across transcripts, 3'/5' end bias, and count of detectable transcripts.
  • Multi-Sample Evaluation: Performs simultaneous assessment of multiple samples to enable comparative analysis of library construction protocols, input materials, and experimental parameters.
  • Modularity and Integration: Provides modular outputs for integration into bioinformatics pipelines and monitoring of alignable read counts, duplication rates, and rRNA contamination.
  • Decision Support for Sample Inclusion: Supplies detailed quality metrics to inform selection or exclusion of samples for downstream analyses.

Scientific Applications:

  • Experiment Design: Evaluates sequencing and library preparation quality to inform experimental setup and protocol selection.
  • Process Optimization: Identifies issues in sample preparation or sequencing runs through targeted quality metrics.
  • Downstream Computational Analysis: Provides quality-filtered inputs and metric-based sample selection to support accurate transcriptome characterization.

Methodology:

Computes the listed RNA-seq quality metrics (yield, alignment and duplication rates, GC bias, rRNA content, region-specific alignment counts, coverage continuity, 3'/5' bias, and detectable transcript counts).

Topics

Details

Tool Type:
command-line tool
Operating Systems:
Linux, Windows, Mac
Programming Languages:
Java
Added:
12/18/2017
Last Updated:
11/24/2024

Operations

Publications

DeLuca DS, Levin JZ, Sivachenko A, Fennell T, Nazaire M, Williams C, Reich M, Winckler W, Getz G. RNA-SeQC: RNA-seq metrics for quality control and process optimization. Bioinformatics. 2012;28(11):1530-1532. doi:10.1093/bioinformatics/bts196. PMID:22539670. PMCID:PMC3356847.

Documentation

Links