SRX5904073 GSM3819834 SRP199576 SRS4824181 GSM3819834 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819834 GSM3819834 GEO Accession GSM3819834 SRX5904074 GSM3819835 SRP199576 SRS4824182 GSM3819835 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819835 GSM3819835 GEO Accession GSM3819835 SRX5904075 GSM3819836 SRP199576 SRS4824183 GSM3819836 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819836 GSM3819836 GEO Accession GSM3819836 SRX5904076 GSM3819837 SRP199576 SRS4824184 GSM3819837 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819837 GSM3819837 GEO Accession GSM3819837 SRX5904077 GSM3819838 SRP199576 SRS4824185 GSM3819838 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819838 GSM3819838 GEO Accession GSM3819838 SRX5904078 GSM3819839 SRP199576 SRS4824186 GSM3819839 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819839 GSM3819839 GEO Accession GSM3819839 SRX5904079 GSM3819840 SRP199576 SRS4824187 GSM3819840 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819840 GSM3819840 GEO Accession GSM3819840 SRX5904080 GSM3819841 SRP199576 SRS4824188 GSM3819841 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819841 GSM3819841 GEO Accession GSM3819841 SRX5904081 GSM3819842 SRP199576 SRS4824189 GSM3819842 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819842 GSM3819842 GEO Accession GSM3819842 SRX5904082 GSM3819843 SRP199576 SRS4824190 GSM3819843 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819843 GSM3819843 GEO Accession GSM3819843 SRX5904083 GSM3819844 SRP199576 SRS4824191 GSM3819844 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819844 GSM3819844 GEO Accession GSM3819844 SRX5904084 GSM3819845 SRP199576 SRS4824192 GSM3819845 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819845 GSM3819845 GEO Accession GSM3819845 SRX5904085 GSM3819846 SRP199576 SRS4824193 GSM3819846 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819846 GSM3819846 GEO Accession GSM3819846 SRX5904086 GSM3819847 SRP199576 SRS4824194 GSM3819847 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819847 GSM3819847 GEO Accession GSM3819847 SRX5904087 GSM3819848 SRP199576 SRS4824195 GSM3819848 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819848 GSM3819848 GEO Accession GSM3819848 SRX5904088 GSM3819849 SRP199576 SRS4824196 GSM3819849 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819849 GSM3819849 GEO Accession GSM3819849 SRX5904089 GSM3819850 SRP199576 SRS4824197 GSM3819850 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819850 GSM3819850 GEO Accession GSM3819850 SRX5904090 GSM3819851 SRP199576 SRS4824198 GSM3819851 RNA-Seq TRANSCRIPTOMIC cDNA Cells were enzymatically dissociated from the aortic root and ascending aorta (to the level of the brachiocephalic artery) of experimental mice Cells were captured on a 10x Chromium instrument (10x Genomics, Pleasanton, CA) using either the V2 or V3 chemistry for 3' whole transcriptome analysis. Manufacturer's instructions for GEM (Gelbead EMulsion) generation, downstream reverse transcription, cDNA isolation, PCR amplification and library preparation were followed without any significant alterations Illumina HiSeq 4000 gds 303819851 GSM3819851 GEO Accession GSM3819851