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Pooling across cells to normalize single-cell RNA sequencing data with many zero counts

Genome biology · 2016 · Vol. 17(1) · pp. 75–75
Aaron T. L. LunKarsten BachJohn C. Marioni

Abstract

Normalization of single-cell RNA sequencing data is necessary to eliminate cell-specific biases prior to downstream analyses. However, this is not straightforward for noisy single-cell data where many counts are zero. We present a novel approach where expression values are summed across pools of cells, and the summed values are used for normalization. Pool-based size factors are then deconvolved to yield cell-based factors. Our deconvolution approach outperforms existing methods for accurate normalization of cell-specific biases in simulated data. Similar behavior is observed in real data, where deconvolution improves the relevance of results of downstream analyses.

Single-cell and spatial transcriptomicsCancer Genomics and DiagnosticsGene expression and cancer classificationNormalization (sociology)PoolingDeconvolutionBiologyComputational biologyRNADatabase normalizationCellBiological systemComputer science

MeSH terms

AlgorithmsAnimalsCalibrationHumansSequence Analysis, RNAGene Expression ProfilingSingle-Cell AnalysisSignal-To-Noise Ratio

Funding

  • Cancer Research UK
Citations
1,276
FWCI
56.57
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