GSM3684659: Young.Z0.66902.B2; Mus musculus; RNA-Seq

SRX5567043 GSM3684659 GSM3684659: Young.Z0.66902.B2; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529985 SAMN11246710 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684659 GSM3684659 GEO Accession GSM3684659 SRX5567044 GSM3684660 GSM3684660: Young.Z0.66919.G4; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529986 SAMN11246709 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684660 GSM3684660 GEO Accession GSM3684660 SRX5567045 GSM3684661 GSM3684661: Young.Z0.66938.D8; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529987 SAMN11246708 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684661 GSM3684661 GEO Accession GSM3684661 SRX5567046 GSM3684679 GSM3684679: Young.SS9hr.66943.D9; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529988 SAMN11246742 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684679 GSM3684679 GEO Accession GSM3684679 SRX5567047 GSM3684680 GSM3684680: Young.SS9hr.66964.D3; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529989 SAMN11246741 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684680 GSM3684680 GEO Accession GSM3684680 SRX5567048 GSM3684681 GSM3684681: Young.SS9hr.66984.F6; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529990 SAMN11246740 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684681 GSM3684681 GEO Accession GSM3684681 SRX5567049 GSM3684682 GSM3684682: Young.SS9hr.67000.B10; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529991 SAMN11246739 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684682 GSM3684682 GEO Accession GSM3684682 SRX5567050 GSM3684683 GSM3684683: Young.SS12hr.66910.D3; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529992 SAMN11246738 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684683 GSM3684683 GEO Accession GSM3684683 SRX5567051 GSM3684684 GSM3684684: Young.SS12hr.66927.C6; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529993 SAMN11246737 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684684 GSM3684684 GEO Accession GSM3684684 SRX5567052 GSM3684685 GSM3684685: Young.SS12hr.66946.B10; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529994 SAMN11246736 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684685 GSM3684685 GEO Accession GSM3684685 SRX5567053 GSM3684686 GSM3684686: Young.SS12hr.66965.E3; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529995 SAMN11246735 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684686 GSM3684686 GEO Accession GSM3684686 SRX5567054 GSM3684687 GSM3684687: Young.SS12hr.66980.B6; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529996 SAMN11246734 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684687 GSM3684687 GEO Accession GSM3684687 SRX5567055 GSM3684688 GSM3684688: Young.SS12hr.67001.C10; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529997 SAMN11246809 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684688 GSM3684688 GEO Accession GSM3684688 SRX5567056 GSM3684689 GSM3684689: Young.SD3hr.66911.E3; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529998 SAMN11246808 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684689 GSM3684689 GEO Accession GSM3684689 SRX5567057 GSM3684690 GSM3684690: Young.SD3hr.66930.F6; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4529999 SAMN11246807 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684690 GSM3684690 GEO Accession GSM3684690 SRX5567058 GSM3684691 GSM3684691: Young.SD3hr.66947.C10; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530000 SAMN11246806 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684691 GSM3684691 GEO Accession GSM3684691 SRX5567059 GSM3684692 GSM3684692: Young.SD3hr.66960.F2; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530001 SAMN11246805 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684692 GSM3684692 GEO Accession GSM3684692 SRX5567060 GSM3684693 GSM3684693: Young.SD3hr.66981.C6; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530002 SAMN11246804 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684693 GSM3684693 GEO Accession GSM3684693 SRX5567061 GSM3684694 GSM3684694: Young.SD3hr.66996.C9; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530003 SAMN11246803 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684694 GSM3684694 GEO Accession GSM3684694 SRX5567062 GSM3684695 GSM3684695: Young.SD6hr.66914.B4; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530004 SAMN11246802 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684695 GSM3684695 GEO Accession GSM3684695 SRX5567063 GSM3684696 GSM3684696: Young.SD6hr.66931.B7; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530005 SAMN11246801 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684696 GSM3684696 GEO Accession GSM3684696 SRX5567064 GSM3684697 GSM3684697: Young.SD6hr.66950.F10; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530006 SAMN11246800 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684697 GSM3684697 GEO Accession GSM3684697 SRX5567065 GSM3684698 GSM3684698: Young.SD6hr.66961.G2; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530007 SAMN11246799 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684698 GSM3684698 GEO Accession GSM3684698 SRX5567066 GSM3684699 GSM3684699: Young.SD6hr.66976.D5; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530008 SAMN11246798 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684699 GSM3684699 GEO Accession GSM3684699 SRX5567067 GSM3684700 GSM3684700: Young.SD6hr.66997.D9; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530009 SAMN11246797 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684700 GSM3684700 GEO Accession GSM3684700 SRX5567068 GSM3684701 GSM3684701: Young.SD9hr.66915.C4; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530010 SAMN11246796 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684701 GSM3684701 GEO Accession GSM3684701 SRX5567069 GSM3684702 GSM3684702: Young.SD9hr.66934.E7; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530011 SAMN11246795 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684702 GSM3684702 GEO Accession GSM3684702 SRX5567070 GSM3684703 GSM3684703: Young.SD9hr.66951.B11; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530012 SAMN11246794 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684703 GSM3684703 GEO Accession GSM3684703 SRX5567071 GSM3684704 GSM3684704: Young.SD9hr.66956.B2; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530013 SAMN11246793 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684704 GSM3684704 GEO Accession GSM3684704 SRX5567072 GSM3684705 GSM3684705: Young.SD9hr.66977.E5; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530014 SAMN11246792 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684705 GSM3684705 GEO Accession GSM3684705 SRX5567073 GSM3684706 GSM3684706: Young.SD9hr.66992.D8; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530015 SAMN11246791 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684706 GSM3684706 GEO Accession GSM3684706 SRX5567074 GSM3684707 GSM3684707: Young.SD12hr.66918.F4; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530016 SAMN11246790 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684707 GSM3684707 GEO Accession GSM3684707 SRX5567075 GSM3684708 GSM3684708: Young.SD12hr.66935.F7; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530017 SAMN11246789 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684708 GSM3684708 GEO Accession GSM3684708 SRX5567076 GSM3684709 GSM3684709: Young.SD12hr.66954.E11; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530018 SAMN11246788 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684709 GSM3684709 GEO Accession GSM3684709 SRX5567077 GSM3684710 GSM3684710: Young.SD12hr.66957.C2; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530019 SAMN11246787 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684710 GSM3684710 GEO Accession GSM3684710 SRX5567078 GSM3684711 GSM3684711: Young.SD12hr.66973.G4; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530020 SAMN11246786 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684711 GSM3684711 GEO Accession GSM3684711 SRX5567079 GSM3684712 GSM3684712: Young.SD12hr.66993.E8; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530021 SAMN11246785 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684712 GSM3684712 GEO Accession GSM3684712 SRX5567080 GSM3684713 GSM3684713: Old.Z0.66904.D2; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530022 SAMN11246784 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684713 GSM3684713 GEO Accession GSM3684713 SRX5567081 GSM3684714 GSM3684714: Old.Z0.66921.C5; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530023 SAMN11246783 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684714 GSM3684714 GEO Accession GSM3684714 SRX5567082 GSM3684715 GSM3684715: Old.Z0.66940.F8; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530024 SAMN11246812 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684715 GSM3684715 GEO Accession GSM3684715 SRX5567083 GSM3684716 GSM3684716: Old.Z0.66974.B5; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530025 SAMN11246811 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684716 GSM3684716 GEO Accession GSM3684716 SRX5567084 GSM3684717 GSM3684717: Old.Z0.66990.B8; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530026 SAMN11246810 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684717 GSM3684717 GEO Accession GSM3684717 SRX5567085 GSM3684718 GSM3684718: Old.Z0.67009.F11; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530027 SAMN11246733 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684718 GSM3684718 GEO Accession GSM3684718 SRX5567086 GSM3684719 GSM3684719: Old.SS3hr.66905.E2; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530028 SAMN11246732 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684719 GSM3684719 GEO Accession GSM3684719 SRX5567087 GSM3684720 GSM3684720: Old.SS3hr.66924.F5; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530029 SAMN11246731 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684720 GSM3684720 GEO Accession GSM3684720 SRX5567088 GSM3684721 GSM3684721: Old.SS3hr.66941.B9; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530030 SAMN11246730 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684721 GSM3684721 GEO Accession GSM3684721 SRX5567089 GSM3684722 GSM3684722: Old.SS3hr.66970.D4; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530031 SAMN11246782 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684722 GSM3684722 GEO Accession GSM3684722 SRX5567090 GSM3684723 GSM3684723: Old.SS3hr.66991.C8; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530032 SAMN11246781 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684723 GSM3684723 GEO Accession GSM3684723 SRX5567091 GSM3684724 GSM3684724: Old.SS3hr.67006.C11; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530033 SAMN11246780 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684724 GSM3684724 GEO Accession GSM3684724 SRX5567092 GSM3684725 GSM3684725: Old.SS6hr.66908.B3; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530034 SAMN11246779 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684725 GSM3684725 GEO Accession GSM3684725 SRX5567093 GSM3684726 GSM3684726: Old.SS6hr.66925.G5; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530035 SAMN11246778 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684726 GSM3684726 GEO Accession GSM3684726 SRX5567094 GSM3684727 GSM3684727: Old.SS6hr.66944.E9; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530036 SAMN11246777 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684727 GSM3684727 GEO Accession GSM3684727 SRX5567095 GSM3684728 GSM3684728: Old.SS6hr.66971.E4; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530037 SAMN11246776 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684728 GSM3684728 GEO Accession GSM3684728 SRX5567096 GSM3684729 GSM3684729: Old.SS6hr.66986.C7; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530038 SAMN11246775 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684729 GSM3684729 GEO Accession GSM3684729 SRX5567097 GSM3684730 GSM3684730: Old.SS6hr.67007.D11; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530039 SAMN11246774 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684730 GSM3684730 GEO Accession GSM3684730 SRX5567098 GSM3684731 GSM3684731: Old.SS9hr.66909.C3; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530040 SAMN11246773 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684731 GSM3684731 GEO Accession GSM3684731 SRX5567099 GSM3684732 GSM3684732: Old.SS9hr.66928.D6; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530041 SAMN11246772 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684732 GSM3684732 GEO Accession GSM3684732 SRX5567100 GSM3684733 GSM3684733: Old.SS9hr.66945.F9; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530042 SAMN11246771 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684733 GSM3684733 GEO Accession GSM3684733 SRX5567101 GSM3684734 GSM3684734: Old.SS9hr.66966.F3; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530043 SAMN11246770 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684734 GSM3684734 GEO Accession GSM3684734 SRX5567102 GSM3684735 GSM3684735: Old.SS9hr.66987.D7; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530044 SAMN11246769 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684735 GSM3684735 GEO Accession GSM3684735 SRX5567103 GSM3684736 GSM3684736: Old.SS9hr.67002.D10; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530045 SAMN11246768 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684736 GSM3684736 GEO Accession GSM3684736 SRX5567104 GSM3684737 GSM3684737: Old.SS12hr.66912.F3; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530046 SAMN11246767 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684737 GSM3684737 GEO Accession GSM3684737 SRX5567105 GSM3684738 GSM3684738: Old.SS12hr.66929.E6; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530047 SAMN11246766 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684738 GSM3684738 GEO Accession GSM3684738 SRX5567106 GSM3684739 GSM3684739: Old.SS12hr.66948.D10; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530048 SAMN11246765 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684739 GSM3684739 GEO Accession GSM3684739 SRX5567107 GSM3684740 GSM3684740: Old.SS12hr.66967.G3; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530049 SAMN11246764 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684740 GSM3684740 GEO Accession GSM3684740 SRX5567108 GSM3684741 GSM3684741: Old.SS12hr.66982.D6; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530050 SAMN11246763 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684741 GSM3684741 GEO Accession GSM3684741 SRX5567109 GSM3684742 GSM3684742: Old.SS12hr.67003.E10; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530051 SAMN11246762 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684742 GSM3684742 GEO Accession GSM3684742 SRX5567110 GSM3684743 GSM3684743: Old.SD3hr.66913.G3; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530052 SAMN11246761 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684743 GSM3684743 GEO Accession GSM3684743 SRX5567111 GSM3684744 GSM3684744: Old.SD3hr.66932.C7; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530053 SAMN11246760 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684744 GSM3684744 GEO Accession GSM3684744 SRX5567112 GSM3684745 GSM3684745: Old.SD3hr.66949.E10; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530054 SAMN11246759 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684745 GSM3684745 GEO Accession GSM3684745 SRX5567113 GSM3684746 GSM3684746: Old.SD3hr.66962.B3; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530055 SAMN11246758 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684746 GSM3684746 GEO Accession GSM3684746 SRX5567114 GSM3684747 GSM3684747: Old.SD3hr.66983.E6; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530056 SAMN11246757 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684747 GSM3684747 GEO Accession GSM3684747 SRX5567115 GSM3684748 GSM3684748: Old.SD3hr.66998.E9; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530057 SAMN11246729 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684748 GSM3684748 GEO Accession GSM3684748 SRX5567116 GSM3684749 GSM3684749: Old.SD6hr.66916.D4; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530058 SAMN11246728 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684749 GSM3684749 GEO Accession GSM3684749 SRX5567117 GSM3684750 GSM3684750: Old.SD6hr.66933.D7; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530059 SAMN11246727 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684750 GSM3684750 GEO Accession GSM3684750 SRX5567118 GSM3684751 GSM3684751: Old.SD6hr.66952.C11; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530060 SAMN11246726 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684751 GSM3684751 GEO Accession GSM3684751 SRX5567119 GSM3684752 GSM3684752: Old.SD6hr.66963.C3; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530061 SAMN11246725 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684752 GSM3684752 GEO Accession GSM3684752 SRX5567120 GSM3684753 GSM3684753: Old.SD6hr.66978.F5; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530062 SAMN11246724 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684753 GSM3684753 GEO Accession GSM3684753 SRX5567121 GSM3684754 GSM3684754: Old.SD6hr.66999.F9; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530063 SAMN11246723 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684754 GSM3684754 GEO Accession GSM3684754 SRX5567122 GSM3684755 GSM3684755: Old.SD9hr.66917.E4; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530064 SAMN11246722 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684755 GSM3684755 GEO Accession GSM3684755 SRX5567123 GSM3684756 GSM3684756: Old.SD9hr.66936.B8; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530065 SAMN11246721 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684756 GSM3684756 GEO Accession GSM3684756 SRX5567124 GSM3684757 GSM3684757: Old.SD9hr.66953.D11; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530066 SAMN11246720 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684757 GSM3684757 GEO Accession GSM3684757 SRX5567125 GSM3684758 GSM3684758: Old.SD9hr.66958.D2; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530067 SAMN11246719 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684758 GSM3684758 GEO Accession GSM3684758 SRX5567126 GSM3684759 GSM3684759: Old.SD9hr.66979.G5; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530068 SAMN11246718 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684759 GSM3684759 GEO Accession GSM3684759 SRX5567127 GSM3684760 GSM3684760: Old.SD9hr.66995.B9; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530069 SAMN11246717 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684760 GSM3684760 GEO Accession GSM3684760 SRX5567128 GSM3684761 GSM3684761: Old.SD12hr.66920.B5; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530070 SAMN11246716 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684761 GSM3684761 GEO Accession GSM3684761 SRX5567129 GSM3684762 GSM3684762: Old.SD12hr.66937.C8; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530071 SAMN11246715 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684762 GSM3684762 GEO Accession GSM3684762 SRX5567130 GSM3684763 GSM3684763: Old.SD12hr.66955.F11; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530072 SAMN11246714 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684763 GSM3684763 GEO Accession GSM3684763 SRX5567131 GSM3684764 GSM3684764: Old.SD12hr.66959.E2; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530073 SAMN11246713 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684764 GSM3684764 GEO Accession GSM3684764 SRX5567132 GSM3684765 GSM3684765: Old.SD12hr.66975.C5; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530074 SAMN11246712 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684765 GSM3684765 GEO Accession GSM3684765 SRX5567133 GSM3684766 GSM3684766: Old.SD12hr.66994.F8; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530075 SAMN11246711 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684766 GSM3684766 GEO Accession GSM3684766 SRX5567134 GSM3684662 GSM3684662: Young.Z0.66972.F4; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530076 SAMN11246707 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684662 GSM3684662 GEO Accession GSM3684662 SRX5567135 GSM3684663 GSM3684663: Young.Z0.66988.E7; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530077 SAMN11246706 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684663 GSM3684663 GEO Accession GSM3684663 SRX5567136 GSM3684664 GSM3684664: Young.Z0.67008.E11; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530078 SAMN11246705 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684664 GSM3684664 GEO Accession GSM3684664 SRX5567137 GSM3684665 GSM3684665: Young.SS3hr.66903.C2; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530079 SAMN11246756 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684665 GSM3684665 GEO Accession GSM3684665 SRX5567138 GSM3684666 GSM3684666: Young.SS3hr.66922.D5; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530080 SAMN11246755 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684666 GSM3684666 GEO Accession GSM3684666 SRX5567139 GSM3684667 GSM3684667: Young.SS3hr.66939.E8; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530081 SAMN11246754 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684667 GSM3684667 GEO Accession GSM3684667 SRX5567140 GSM3684668 GSM3684668: Young.SS3hr.66968.B4; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530082 SAMN11246753 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684668 GSM3684668 GEO Accession GSM3684668 SRX5567141 GSM3684669 GSM3684669: Young.SS3hr.66989.F7; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530083 SAMN11246752 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684669 GSM3684669 GEO Accession GSM3684669 SRX5567142 GSM3684670 GSM3684670: Young.SS3hr.67005.B11; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530084 SAMN11246751 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684670 GSM3684670 GEO Accession GSM3684670 SRX5567143 GSM3684671 GSM3684671: Young.SS6hr.66906.F2; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530085 SAMN11246750 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684671 GSM3684671 GEO Accession GSM3684671 SRX5567144 GSM3684672 GSM3684672: Young.SS6hr.66923.E5; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530086 SAMN11246749 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684672 GSM3684672 GEO Accession GSM3684672 SRX5567145 GSM3684673 GSM3684673: Young.SS6hr.66942.C9; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530087 SAMN11246748 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684673 GSM3684673 GEO Accession GSM3684673 SRX5567146 GSM3684674 GSM3684674: Young.SS6hr.66969.C4; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530088 SAMN11246747 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684674 GSM3684674 GEO Accession GSM3684674 SRX5567147 GSM3684675 GSM3684675: Young.SS6hr.66985.B7; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530089 SAMN11246746 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684675 GSM3684675 GEO Accession GSM3684675 SRX5567148 GSM3684676 GSM3684676: Young.SS6hr.67004.F10; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530090 SAMN11246745 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684676 GSM3684676 GEO Accession GSM3684676 SRX5567149 GSM3684677 GSM3684677: Young.SS9hr.66907.G2; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530092 SAMN11246744 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684677 GSM3684677 GEO Accession GSM3684677 SRX5567150 GSM3684678 GSM3684678: Young.SS9hr.66926.B6; Mus musculus; RNA-Seq SRP189300 PRJNA528862 SRS4530091 SAMN11246743 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized, and brains were removed and stored at -80°C. Microdissection of mPFC was performed using micropunch. RNA extraction was performed using an RNAqueous-Micro Kit and genome DNA was removed with RNase-Free DNase. Total RNA from each sample was prepared for sequencing using the Illumina: TruSeq Stranded mRNA Sample Preparation Kit. 200 ng of RNA was used to prepare the RNA libraries. The libraries were sequenced on Illumina HiSeq 4000. Depths of 19-32 million single 100bp reads were generated for each sample. Illumina HiSeq 4000 gds 303684678 GSM3684678 GEO Accession GSM3684678