SRX3481782 GSM2893737 SRP127005 SRS2767598 GSM2893737 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893737 GSM2893737 GEO Accession GSM2893737 SRX3481783 GSM2893738 SRP127005 SRS2767599 GSM2893738 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893738 GSM2893738 GEO Accession GSM2893738 SRX3481784 GSM2893739 SRP127005 SRS2767608 GSM2893739 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893739 GSM2893739 GEO Accession GSM2893739 SRX3481785 GSM2893740 SRP127005 SRS2767600 GSM2893740 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893740 GSM2893740 GEO Accession GSM2893740 SRX3481786 GSM2893741 SRP127005 SRS2767601 GSM2893741 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893741 GSM2893741 GEO Accession GSM2893741 SRX3481787 GSM2893742 SRP127005 SRS2767602 GSM2893742 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893742 GSM2893742 GEO Accession GSM2893742 SRX3481788 GSM2893743 SRP127005 SRS2767603 GSM2893743 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893743 GSM2893743 GEO Accession GSM2893743 SRX3481789 GSM2893744 SRP127005 SRS2767616 GSM2893744 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893744 GSM2893744 GEO Accession GSM2893744 SRX3481790 GSM2893745 SRP127005 SRS2767605 GSM2893745 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893745 GSM2893745 GEO Accession GSM2893745 SRX3481791 GSM2893746 SRP127005 SRS2767606 GSM2893746 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893746 GSM2893746 GEO Accession GSM2893746 SRX3481792 GSM2893747 SRP127005 SRS2767607 GSM2893747 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893747 GSM2893747 GEO Accession GSM2893747 SRX3481793 GSM2893748 SRP127005 SRS2767618 GSM2893748 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893748 GSM2893748 GEO Accession GSM2893748 SRX3481794 GSM2893749 SRP127005 SRS2767609 GSM2893749 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893749 GSM2893749 GEO Accession GSM2893749 SRX3481795 GSM2893750 SRP127005 SRS2767619 GSM2893750 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893750 GSM2893750 GEO Accession GSM2893750 SRX3481796 GSM2893751 SRP127005 SRS2767612 GSM2893751 RNA-Seq TRANSCRIPTOMIC cDNA Mice were euthanized under anesthesia and cerebella were quickly dissected over ice. RNA was extracted following published protocols. Isolated RNA was submitted to the University of Minnesota Genomics Center. Sample quality checks using the NanoDrop spectrophotometer and Agilent Bioanalyzer 2100 were conducted. Using NuGEN Ovation RNA-Seq System v2, purified double-stranded cDNA was generated from 10 ng of total RNA and amplified using both 3' poly (A) selection and random priming. 2 µg of each sample was sheared using the Covaris S2 focused-ultrasonicator following the manufacturer's protocol to obtain a final library with insert size of 400 bp. The sheared samples were quantified using the NanoDrop ND-1000 spectrophotometer and Invitrogen Qubit 2.0 DNA quantitation assay. The fragment sizes were confirmed on the Agilent Bioanalyzer to verify proper shearing. A double-stranded DNA library was produced using Illumina TruSeq DNA library preparation system and the sequencing was run on a HiSeq 2500 system. Illumina HiSeq 2000 gds 302893751 GSM2893751 GEO Accession GSM2893751