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Linnorm: improved statistical analysis for single cell RNA-seq expression data
Author(s) -
Shun H. Yip,
Panwen Wang,
Jean-Pierre A. Kocher,
Pak C. Sham,
Junwen Wang
Publication year - 2017
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkx828
Subject(s) - normalization (sociology) , biology , cluster analysis , rna seq , computational biology , statistical analysis , transformation (genetics) , data mining , computer science , data transformation , bioinformatics , artificial intelligence , statistics , transcriptome , genetics , gene expression , gene , mathematics , sociology , anthropology , data warehouse
Linnorm is a novel normalization and transformation method for the analysis of single cell RNA sequencing (scRNA-seq) data. Linnorm is developed to remove technical noises and simultaneously preserve biological variations in scRNA-seq data, such that existing statistical methods can be improved. Using real scRNA-seq data, we compared Linnorm with existing normalization methods, including NODES, SAMstrt, SCnorm, scran, DESeq and TMM. Linnorm shows advantages in speed, technical noise removal and preservation of cell heterogeneity, which can improve existing methods in the discovery of novel subtypes, pseudo-temporal ordering of cells, clustering analysis, etc. Linnorm also performs better than existing DEG analysis methods, including BASiCS, NODES, SAMstrt, Seurat and DESeq2, in false positive rate control and accuracy.

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