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A survey of best practices for RNA-seq data analysis

Genome biology · 2016 · Vol. 17(1) · pp. 13–13
Ana ConesaPedro MadrigalSonia TarazonaDavid Gómez-CabreroAlejandra CerveraAndrew McPhersonMichał Wojciech SzcześniakDaniel J. GaffneyLaura L. EloXuegong ZhangA Mortazavi

Abstract

RNA-sequencing (RNA-seq) has a wide variety of applications, but no single analysis pipeline can be used in all cases. We review all of the major steps in RNA-seq data analysis, including experimental design, quality control, read alignment, quantification of gene and transcript levels, visualization, differential gene expression, alternative splicing, functional analysis, gene fusion detection and eQTL mapping. We highlight the challenges associated with each step. We discuss the analysis of small RNAs and the integration of RNA-seq with other functional genomics techniques. Finally, we discuss the outlook for novel technologies that are changing the state of the art in transcriptomics.

Genomics and Phylogenetic StudiesCancer-related molecular mechanisms researchRNA modifications and cancerRNA-SeqBiologyComputational biologyExpression quantitative trait lociTranscriptomeFunctional genomicsGenomicsRNARNA splicingAlternative splicing

MeSH terms

Base SequenceRNASoftwareAlternative SplicingSequence Analysis, RNAGene Expression ProfilingGenomicsGene FusionHigh-Throughput Nucleotide Sequencing

Funding

  • Helsingin Yliopisto
  • Wellcome Trust
  • Academy of Finland
  • Karolinska Institutet
  • Tsinghua University
  • Simon Fraser University
  • Tsinghua National Laboratory for Information Science and Technology
  • Turun Yliopisto
  • Sigrid Juséliuksen Säätiö
  • Åbo Akademi
  • Science for Life Laboratory
  • Uniwersytet im. Adama Mickiewicza w Poznaniu
  • Medical Research Council
  • Seventh Framework Programme
  • European Regional Development Fund
  • National Key Research and Development Program of China
Citations
2,822
FWCI
158.75
field-weighted impact
References
214
Percentile
100%
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