Normalization and noise reduction for single cell RNA-seq experiments

Bioinformatics. 2015 Jul 1;31(13):2225-7. doi: 10.1093/bioinformatics/btv122. Epub 2015 Feb 24.

Abstract

A major roadblock towards accurate interpretation of single cell RNA-seq data is large technical noise resulted from small amount of input materials. The existing methods mainly aim to find differentially expressed genes rather than directly de-noise the single cell data. We present here a powerful but simple method to remove technical noise and explicitly compute the true gene expression levels based on spike-in ERCC molecules.

Availability and implementation: The software is implemented by R and the download version is available at http://wanglab.ucsd.edu/star/GRM.

Contact: wei-wang@ucsd.edu

Supplementary information: Supplementary data are available at Bioinformatics online.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Gene Expression Profiling / methods*
  • High-Throughput Nucleotide Sequencing / methods*
  • Humans
  • Sequence Analysis, RNA / methods*
  • Signal-To-Noise Ratio
  • Single-Cell Analysis / methods*
  • Software*
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