SRX12752323 GSM5652634 SRP342864 SRS10700000 GSM5652634 RNA-Seq TRANSCRIPTOMIC cDNA Mouse hearts were harvested and digested by collagenase to single cell suspension. Neutrophils were sorted by flow cytometry. Dead cells were excluded by live-dead dye staining. RNA was extratced from neutrophils by a Qiagen RNeasy micro kit and subjected to RNA-seq using paired-end sequencing. RNA libraries were prepared for sequencing using the SMART-Seq v4 for CDNA and the Nextera XT kit for library creation NextSeq 550 gds 305652634 GSM5652634 GEO Accession GSM5652634 SRX12752324 GSM5652635 SRP342864 SRS10700002 GSM5652635 RNA-Seq TRANSCRIPTOMIC cDNA Mouse hearts were harvested and digested by collagenase to single cell suspension. Neutrophils were sorted by flow cytometry. Dead cells were excluded by live-dead dye staining. RNA was extratced from neutrophils by a Qiagen RNeasy micro kit and subjected to RNA-seq using paired-end sequencing. RNA libraries were prepared for sequencing using the SMART-Seq v4 for CDNA and the Nextera XT kit for library creation NextSeq 550 gds 305652635 GSM5652635 GEO Accession GSM5652635 SRX12752325 GSM5652636 SRP342864 SRS10700001 GSM5652636 RNA-Seq TRANSCRIPTOMIC cDNA Mouse hearts were harvested and digested by collagenase to single cell suspension. Neutrophils were sorted by flow cytometry. Dead cells were excluded by live-dead dye staining. RNA was extratced from neutrophils by a Qiagen RNeasy micro kit and subjected to RNA-seq using paired-end sequencing. RNA libraries were prepared for sequencing using the SMART-Seq v4 for CDNA and the Nextera XT kit for library creation NextSeq 550 gds 305652636 GSM5652636 GEO Accession GSM5652636 SRX12752326 GSM5652637 SRP342864 SRS10700003 GSM5652637 RNA-Seq TRANSCRIPTOMIC cDNA Mouse hearts were harvested and digested by collagenase to single cell suspension. Neutrophils were sorted by flow cytometry. Dead cells were excluded by live-dead dye staining. RNA was extratced from neutrophils by a Qiagen RNeasy micro kit and subjected to RNA-seq using paired-end sequencing. RNA libraries were prepared for sequencing using the SMART-Seq v4 for CDNA and the Nextera XT kit for library creation NextSeq 550 gds 305652637 GSM5652637 GEO Accession GSM5652637 SRX12752327 GSM5652638 SRP342864 SRS10700004 GSM5652638 RNA-Seq TRANSCRIPTOMIC cDNA Mouse hearts were harvested and digested by collagenase to single cell suspension. Neutrophils were sorted by flow cytometry. Dead cells were excluded by live-dead dye staining. RNA was extratced from neutrophils by a Qiagen RNeasy micro kit and subjected to RNA-seq using paired-end sequencing. RNA libraries were prepared for sequencing using the SMART-Seq v4 for CDNA and the Nextera XT kit for library creation NextSeq 550 gds 305652638 GSM5652638 GEO Accession GSM5652638 SRX12752328 GSM5652639 SRP342864 SRS10700005 GSM5652639 RNA-Seq TRANSCRIPTOMIC cDNA Mouse hearts were harvested and digested by collagenase to single cell suspension. Neutrophils were sorted by flow cytometry. Dead cells were excluded by live-dead dye staining. RNA was extratced from neutrophils by a Qiagen RNeasy micro kit and subjected to RNA-seq using paired-end sequencing. RNA libraries were prepared for sequencing using the SMART-Seq v4 for CDNA and the Nextera XT kit for library creation NextSeq 550 gds 305652639 GSM5652639 GEO Accession GSM5652639 SRX12752329 GSM5652640 SRP342864 SRS10700006 GSM5652640 RNA-Seq TRANSCRIPTOMIC cDNA Mouse hearts were harvested and digested by collagenase to single cell suspension. Neutrophils were sorted by flow cytometry. Dead cells were excluded by live-dead dye staining. RNA was extratced from neutrophils by a Qiagen RNeasy micro kit and subjected to RNA-seq using paired-end sequencing. RNA libraries were prepared for sequencing using the SMART-Seq v4 for CDNA and the Nextera XT kit for library creation NextSeq 550 gds 305652640 GSM5652640 GEO Accession GSM5652640 SRX12752330 GSM5652641 SRP342864 SRS10700007 GSM5652641 RNA-Seq TRANSCRIPTOMIC cDNA Mouse hearts were harvested and digested by collagenase to single cell suspension. Neutrophils were sorted by flow cytometry. Dead cells were excluded by live-dead dye staining. RNA was extratced from neutrophils by a Qiagen RNeasy micro kit and subjected to RNA-seq using paired-end sequencing. RNA libraries were prepared for sequencing using the SMART-Seq v4 for CDNA and the Nextera XT kit for library creation NextSeq 550 gds 305652641 GSM5652641 GEO Accession GSM5652641