RNA-SeQC: RNA-seq metrics for quality control and process optimization

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ID: 301750
2012
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Abstract
Abstract Summary: RNA-seq, the application of next-generation sequencing to RNA, provides transcriptome-wide characterization of cellular activity. Assessment of sequencing performance and library quality is critical to the interpretation of RNA-seq data, yet few tools exist to address this issue. We introduce RNA-SeQC, a program which provides key measures of data quality. These metrics include yield, alignment and duplication rates; GC bias, rRNA content, regions of alignment (exon, intron and intragenic), continuity of coverage, 3′/5′ bias and count of detectable transcripts, among others. The software provides multi-sample evaluation of library construction protocols, input materials and other experimental parameters. The modularity of the software enables pipeline integration and the routine monitoring of key measures of data quality such as the number of alignable reads, duplication rates and rRNA contamination. RNA-SeQC allows investigators to make informed decisions about sample inclusion in downstream analysis. In summary, RNA-SeQC provides quality control measures critical to experiment design, process optimization and downstream computational analysis. Availability and implementation: See www.genepattern.org to run online, or www.broadinstitute.org/rna-seqc/ for a command line tool. Contact: ddeluca@broadinstitute.org Supplementary information: Supplementary data are available at Bioinformatics online.
Reference Key
openalex_W2160443244 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors David S. DeLuca, Joshua Z. Levin, Andrey Sivachenko, Timothy R. Fennell, Marc-Danie Nazaire, Chris Williams, Michael Reich, Wendy Winckler, Gad Getz
Journal BMC Bioinformatics
Year 2012
DOI
10.1093/bioinformatics/bts196
URL
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