article Open AccessTop 1% cited
Differential expression analysis for sequence count data
Genome biology · 2010 · Vol. 11(10) · pp. R106–R106
Simon Anders✉(European Molecular Biology Laboratory)Wolfgang Huber(European Molecular Biology Laboratory)
Abstract
High-throughput sequencing assays such as RNA-Seq, ChIP-Seq or barcode counting provide quantitative readouts in the form of count data. To infer differential signal in such data correctly and with good statistical power, estimation of data variability throughout the dynamic range and a suitable error model are required. We propose a method based on the negative binomial distribution, with variance and mean linked by local regression and present an implementation, DESeq, as an R/Bioconductor package.
Gene expression and cancer classificationMolecular Biology Techniques and ApplicationsRNA Research and SplicingBioconductorCount dataNegative binomial distributionBarcodeBiologyStatisticsBinomial distributionComputational biologyComputer scienceMathematics
MeSH terms
AnimalsDrosophilaModels, GeneticSaccharomyces cerevisiaeStem CellsBinomial DistributionLinear ModelsSequence Analysis, RNAComputational BiologyGene Expression ProfilingTissue Culture TechniquesChromatin ImmunoprecipitationHigh-Throughput Nucleotide Sequencing
Funding
- European Commission
Citations
16,273
FWCI
136.86
field-weighted impact
References
49
Percentile
100%
vs. same field & year
Citations per year
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