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Table 2 Overview of processing of cells and RNA for RNA-seq data sets analyzed in this study

From: A map of gene expression in neutrophil-like cell lines

Data set

Neutrophil isolation

RNA enrichment

Sequencing method

Read mapping and analysis

this study

N/A

polyA enrichment

Illimuna HiSeq, 1 × 75 bp

All data sets were reanalyzed in this study with uniform read mapping and analysis methods. See Methods for details

Cusanovich et al

N/A

polyA enrichment

Illumina NextSeq, 1 × 75 bp

Jiang et al

density gradient sedimentation (Polymorphprep)

polyA enrichment

Illumina HiSeq, 2 × 75 bp paired end

Thomas et al. (samples 1 and 3)

negative selection

polyA enrichment

Illimuna HiSeq, 1 × 50 bp

Thomas et al. (samples 2 and 4)

density gradient sedimentation (Polymorphprep)

polyA enrichment

Illimuna HiSeq, 1 × 50 bp

Wright et al

density gradient sedimentation (Polymorphprep)

polyA enrichment

Illimuna HiSeq, 1 × 50 bp

Taylor et al

density gradient sedimentation (Percoll)

polyA enrichment

Illimuna HiSeq, 1 × 50 bp

Coffelt et al

positive selection (Ly6G+)

polyA enrichment

Illimuna HiSeq, 1 × 50 bp

  1. The methods of neutrophil isolation (for studies involving primary neutrophils), mRNA enrichment, and sequencing are indicated in the table. All data sets were re-analyzed with a uniform computational pipeline (see Methods for details) to avoid potential systematic differences due to analysis methods