SRX5611582 GSM3689774 SRP189993 PRJNA529656 SRS4559259 SAMN11280503 RNA-Seq TRANSCRIPTOMIC cDNA CD45+ innate immune cells (T/B cell negative CD45+ cells) were sorted using a BD FACS AriaII. Live single cells were loaded into the 10x genomics machine. Full length cDNA libraries were prepared by incubation of Gel Bead-In-EMulsions (GEMs) in a thermocycler machine with Chromium v2. GEMs containing cDNAs were broken and all single cell cDNA libraries were pooled together, cleaned using DynaBeads MyOne™ Silane beads (Fisher PN 37002D), and pre-amplified by PCR to generate sufficient mass for sequencing library construction. NextSeq 500 gds 303689774 GSM3689774 GEO Accession GSM3689774 SRX5611583 GSM3689775 SRP189993 PRJNA529656 SRS4559260 SAMN11280502 RNA-Seq TRANSCRIPTOMIC cDNA CD45+ innate immune cells (T/B cell negative CD45+ cells) were sorted using a BD FACS AriaII. Live single cells were loaded into the 10x genomics machine. Full length cDNA libraries were prepared by incubation of Gel Bead-In-EMulsions (GEMs) in a thermocycler machine with Chromium v2. GEMs containing cDNAs were broken and all single cell cDNA libraries were pooled together, cleaned using DynaBeads MyOne™ Silane beads (Fisher PN 37002D), and pre-amplified by PCR to generate sufficient mass for sequencing library construction. NextSeq 500 gds 303689775 GSM3689775 GEO Accession GSM3689775 SRX5611584 GSM3689776 SRP189993 PRJNA529656 SRS4559261 SAMN11280505 RNA-Seq TRANSCRIPTOMIC cDNA CD45+ innate immune cells (T/B cell negative CD45+ cells) were sorted using a BD FACS AriaII. Live single cells were loaded into the 10x genomics machine. Full length cDNA libraries were prepared by incubation of Gel Bead-In-EMulsions (GEMs) in a thermocycler machine with Chromium v2. GEMs containing cDNAs were broken and all single cell cDNA libraries were pooled together, cleaned using DynaBeads MyOne™ Silane beads (Fisher PN 37002D), and pre-amplified by PCR to generate sufficient mass for sequencing library construction. NextSeq 500 gds 303689776 GSM3689776 GEO Accession GSM3689776 SRX5611585 GSM3689777 SRP189993 PRJNA529656 SRS4559262 SAMN11280504 RNA-Seq TRANSCRIPTOMIC cDNA CD45+ innate immune cells (T/B cell negative CD45+ cells) were sorted using a BD FACS AriaII. Live single cells were loaded into the 10x genomics machine. Full length cDNA libraries were prepared by incubation of Gel Bead-In-EMulsions (GEMs) in a thermocycler machine with Chromium v2. GEMs containing cDNAs were broken and all single cell cDNA libraries were pooled together, cleaned using DynaBeads MyOne™ Silane beads (Fisher PN 37002D), and pre-amplified by PCR to generate sufficient mass for sequencing library construction. NextSeq 500 gds 303689777 GSM3689777 GEO Accession GSM3689777