SRX5276001 GSM3573756 SRP181125 SRS4276132 GSM3573756 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573756 GSM3573756 GEO Accession GSM3573756 SRX5276002 GSM3573757 SRP181125 SRS4276133 GSM3573757 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573757 GSM3573757 GEO Accession GSM3573757 SRX5276003 GSM3573758 SRP181125 SRS4276134 GSM3573758 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573758 GSM3573758 GEO Accession GSM3573758 SRX5276004 GSM3573759 SRP181125 SRS4276135 GSM3573759 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573759 GSM3573759 GEO Accession GSM3573759 SRX5276005 GSM3573760 SRP181125 SRS4276137 GSM3573760 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573760 GSM3573760 GEO Accession GSM3573760 SRX5276006 GSM3573761 SRP181125 SRS4276136 GSM3573761 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573761 GSM3573761 GEO Accession GSM3573761 SRX5276007 GSM3573762 SRP181125 SRS4276138 GSM3573762 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573762 GSM3573762 GEO Accession GSM3573762 SRX5276008 GSM3573763 SRP181125 SRS4276139 GSM3573763 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573763 GSM3573763 GEO Accession GSM3573763 SRX5276009 GSM3573764 SRP181125 SRS4276140 GSM3573764 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573764 GSM3573764 GEO Accession GSM3573764 SRX5276010 GSM3573765 SRP181125 SRS4276141 GSM3573765 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573765 GSM3573765 GEO Accession GSM3573765 SRX5276011 GSM3573766 SRP181125 SRS4276143 GSM3573766 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573766 GSM3573766 GEO Accession GSM3573766 SRX5276012 GSM3573767 SRP181125 SRS4276142 GSM3573767 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573767 GSM3573767 GEO Accession GSM3573767 SRX5276013 GSM3573768 SRP181125 SRS4276144 GSM3573768 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573768 GSM3573768 GEO Accession GSM3573768 SRX5276014 GSM3573769 SRP181125 SRS4276145 GSM3573769 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573769 GSM3573769 GEO Accession GSM3573769 SRX5276015 GSM3573770 SRP181125 SRS4276146 GSM3573770 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573770 GSM3573770 GEO Accession GSM3573770 SRX5276016 GSM3573771 SRP181125 SRS4276147 GSM3573771 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573771 GSM3573771 GEO Accession GSM3573771 SRX5276017 GSM3573772 SRP181125 SRS4276149 GSM3573772 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573772 GSM3573772 GEO Accession GSM3573772 SRX5276018 GSM3573773 SRP181125 SRS4276148 GSM3573773 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573773 GSM3573773 GEO Accession GSM3573773 SRX5276019 GSM3573774 SRP181125 SRS4276151 GSM3573774 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573774 GSM3573774 GEO Accession GSM3573774 SRX5276020 GSM3573775 SRP181125 SRS4276150 GSM3573775 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573775 GSM3573775 GEO Accession GSM3573775 SRX5276021 GSM3573776 SRP181125 SRS4276152 GSM3573776 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573776 GSM3573776 GEO Accession GSM3573776 SRX5276022 GSM3573777 SRP181125 SRS4276153 GSM3573777 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573777 GSM3573777 GEO Accession GSM3573777 SRX5276023 GSM3573778 SRP181125 SRS4276154 GSM3573778 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573778 GSM3573778 GEO Accession GSM3573778 SRX5276024 GSM3573779 SRP181125 SRS4276155 GSM3573779 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573779 GSM3573779 GEO Accession GSM3573779 SRX5276025 GSM3573780 SRP181125 SRS4276156 GSM3573780 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573780 GSM3573780 GEO Accession GSM3573780 SRX5276026 GSM3573781 SRP181125 SRS4276157 GSM3573781 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573781 GSM3573781 GEO Accession GSM3573781 SRX5276027 GSM3573782 SRP181125 SRS4276159 GSM3573782 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573782 GSM3573782 GEO Accession GSM3573782 SRX5276028 GSM3573783 SRP181125 SRS4276158 GSM3573783 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573783 GSM3573783 GEO Accession GSM3573783 SRX5276029 GSM3573784 SRP181125 SRS4276160 GSM3573784 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573784 GSM3573784 GEO Accession GSM3573784 SRX5276030 GSM3573785 SRP181125 SRS4276161 GSM3573785 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573785 GSM3573785 GEO Accession GSM3573785 SRX5276031 GSM3573786 SRP181125 SRS4276162 GSM3573786 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573786 GSM3573786 GEO Accession GSM3573786 SRX5276032 GSM3573787 SRP181125 SRS4276163 GSM3573787 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573787 GSM3573787 GEO Accession GSM3573787 SRX5276033 GSM3573788 SRP181125 SRS4276165 GSM3573788 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573788 GSM3573788 GEO Accession GSM3573788 SRX5276034 GSM3573789 SRP181125 SRS4276164 GSM3573789 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573789 GSM3573789 GEO Accession GSM3573789 SRX5276035 GSM3573790 SRP181125 SRS4276166 GSM3573790 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573790 GSM3573790 GEO Accession GSM3573790 SRX5276036 GSM3573791 SRP181125 SRS4276167 GSM3573791 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573791 GSM3573791 GEO Accession GSM3573791 SRX5276037 GSM3573792 SRP181125 SRS4276168 GSM3573792 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573792 GSM3573792 GEO Accession GSM3573792 SRX5276038 GSM3573793 SRP181125 SRS4276169 GSM3573793 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573793 GSM3573793 GEO Accession GSM3573793 SRX5276039 GSM3573794 SRP181125 SRS4276170 GSM3573794 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573794 GSM3573794 GEO Accession GSM3573794 SRX5276040 GSM3573795 SRP181125 SRS4276171 GSM3573795 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573795 GSM3573795 GEO Accession GSM3573795 SRX5276041 GSM3573796 SRP181125 SRS4276172 GSM3573796 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573796 GSM3573796 GEO Accession GSM3573796 SRX5276042 GSM3573797 SRP181125 SRS4276173 GSM3573797 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573797 GSM3573797 GEO Accession GSM3573797 SRX5276043 GSM3573798 SRP181125 SRS4276174 GSM3573798 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573798 GSM3573798 GEO Accession GSM3573798 SRX5276044 GSM3573799 SRP181125 SRS4276175 GSM3573799 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573799 GSM3573799 GEO Accession GSM3573799 SRX5276045 GSM3573800 SRP181125 SRS4276176 GSM3573800 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573800 GSM3573800 GEO Accession GSM3573800 SRX5276046 GSM3573801 SRP181125 SRS4276177 GSM3573801 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573801 GSM3573801 GEO Accession GSM3573801 SRX5276047 GSM3573802 SRP181125 SRS4276178 GSM3573802 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573802 GSM3573802 GEO Accession GSM3573802 SRX5276048 GSM3573803 SRP181125 SRS4276179 GSM3573803 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573803 GSM3573803 GEO Accession GSM3573803 SRX5276049 GSM3573804 SRP181125 SRS4276180 GSM3573804 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573804 GSM3573804 GEO Accession GSM3573804 SRX5276050 GSM3573805 SRP181125 SRS4276181 GSM3573805 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573805 GSM3573805 GEO Accession GSM3573805 SRX5276051 GSM3573806 SRP181125 SRS4276182 GSM3573806 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573806 GSM3573806 GEO Accession GSM3573806 SRX5276052 GSM3573807 SRP181125 SRS4276183 GSM3573807 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573807 GSM3573807 GEO Accession GSM3573807 SRX5276053 GSM3573808 SRP181125 SRS4276184 GSM3573808 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573808 GSM3573808 GEO Accession GSM3573808 SRX5276054 GSM3573809 SRP181125 SRS4276185 GSM3573809 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573809 GSM3573809 GEO Accession GSM3573809 SRX5276055 GSM3573810 SRP181125 SRS4276186 GSM3573810 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573810 GSM3573810 GEO Accession GSM3573810 SRX5276056 GSM3573811 SRP181125 SRS4276187 GSM3573811 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573811 GSM3573811 GEO Accession GSM3573811 SRX5276057 GSM3573812 SRP181125 SRS4276188 GSM3573812 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573812 GSM3573812 GEO Accession GSM3573812 SRX5276058 GSM3573813 SRP181125 SRS4276189 GSM3573813 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573813 GSM3573813 GEO Accession GSM3573813 SRX5276059 GSM3573814 SRP181125 SRS4276190 GSM3573814 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573814 GSM3573814 GEO Accession GSM3573814 SRX5276060 GSM3573815 SRP181125 SRS4276191 GSM3573815 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573815 GSM3573815 GEO Accession GSM3573815 SRX5276061 GSM3573816 SRP181125 SRS4276192 GSM3573816 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573816 GSM3573816 GEO Accession GSM3573816 SRX5276062 GSM3573817 SRP181125 SRS4276193 GSM3573817 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573817 GSM3573817 GEO Accession GSM3573817 SRX5276063 GSM3573818 SRP181125 SRS4276194 GSM3573818 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573818 GSM3573818 GEO Accession GSM3573818 SRX5276064 GSM3573819 SRP181125 SRS4276195 GSM3573819 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573819 GSM3573819 GEO Accession GSM3573819 SRX5276065 GSM3573820 SRP181125 SRS4276196 GSM3573820 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573820 GSM3573820 GEO Accession GSM3573820 SRX5276066 GSM3573821 SRP181125 SRS4276197 GSM3573821 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573821 GSM3573821 GEO Accession GSM3573821 SRX5276067 GSM3573822 SRP181125 SRS4276198 GSM3573822 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573822 GSM3573822 GEO Accession GSM3573822 SRX5276068 GSM3573823 SRP181125 SRS4276199 GSM3573823 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573823 GSM3573823 GEO Accession GSM3573823 SRX5276069 GSM3573824 SRP181125 SRS4276200 GSM3573824 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573824 GSM3573824 GEO Accession GSM3573824 SRX5276070 GSM3573825 SRP181125 SRS4276201 GSM3573825 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573825 GSM3573825 GEO Accession GSM3573825 SRX5276071 GSM3573826 SRP181125 SRS4276203 GSM3573826 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573826 GSM3573826 GEO Accession GSM3573826 SRX5276072 GSM3573827 SRP181125 SRS4276202 GSM3573827 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573827 GSM3573827 GEO Accession GSM3573827 SRX5276073 GSM3573828 SRP181125 SRS4276205 GSM3573828 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573828 GSM3573828 GEO Accession GSM3573828 SRX5276074 GSM3573829 SRP181125 SRS4276204 GSM3573829 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573829 GSM3573829 GEO Accession GSM3573829 SRX5276075 GSM3573830 SRP181125 SRS4276207 GSM3573830 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573830 GSM3573830 GEO Accession GSM3573830 SRX5276076 GSM3573831 SRP181125 SRS4276206 GSM3573831 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573831 GSM3573831 GEO Accession GSM3573831 SRX5276077 GSM3573832 SRP181125 SRS4276209 GSM3573832 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573832 GSM3573832 GEO Accession GSM3573832 SRX5276078 GSM3573833 SRP181125 SRS4276208 GSM3573833 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573833 GSM3573833 GEO Accession GSM3573833 SRX5276079 GSM3573834 SRP181125 SRS4276210 GSM3573834 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573834 GSM3573834 GEO Accession GSM3573834 SRX5276080 GSM3573835 SRP181125 SRS4276211 GSM3573835 RNA-Seq TRANSCRIPTOMIC cDNA Brain samples were harvested on the same day and snap frozen in RNA later solution (Ambion), within a two-hour window. Frozen brain tissue was shipped to FSU.RNA and protein were extracted from the frozen brain tissue using the NucleoSpin RNA/Protein purification kit (Macherey-Nagel). The brain tissue was homogenized using a motorized homogenizer 1 ug of total RNA was used for subsequent mRNA isolation (New England Biolabs Inc. PolyA magnetic mRNA isolation kit). The External RNA Controls Consortium (ERCC) RNA Spike-in Controls (Ambion 4456740) were diluted 1:100 and added to total RNA before mRNA isolation. RNA-seq libraries were generated using the NEBNext Ultra RNA Library Prep Kit for Illumina (New England Biolabs Inc. E7530L). The qualities of the libraries were examined using Agilent High Sensitivity DNA Bioanalyzer Chips (Agilent Technologies 5067-4626) and quantified by KAPA Library Quantification Kits Libraries were sequenced on an Illumina 2500 platform, single end, 100 base reads. Illumina HiSeq 2500 gds 303573835 GSM3573835 GEO Accession GSM3573835