SRX3035853 GSM2717951 SRP113587 SRS2384330 GSM2717951 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from freshly dissected cerebella using Trizol (Invitrogen, CA, USA) according to the manufacturer’s instructions after homogenization by a Bullet Blender (Next Advance) and followed by isopropanol precipitation. Residual genomic DNA was removed using the Turbo DNA-free kit (Ambion®,Invitrogen, CA, USA). RNA integrity and absence of DNA was confirmed by Bioanalyzer RNA Nano chips (Agilent, RIN > 9.3) and Qubit DNA High sensitivity kit, respectively. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation HT Kit following the standard protocol starting from 4 μg of total RNA using 11 cycles of PCR amplification. Sequencing was performed on 2 lanes of an Illumina HiSeq4000 (Illumina, CA, USA) multiplexing all samples. Illumina HiSeq 4000 gds 302717951 GSM2717951 GEO Accession GSM2717951 SRX3035854 GSM2717952 SRP113587 SRS2384329 GSM2717952 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from freshly dissected cerebella using Trizol (Invitrogen, CA, USA) according to the manufacturer’s instructions after homogenization by a Bullet Blender (Next Advance) and followed by isopropanol precipitation. Residual genomic DNA was removed using the Turbo DNA-free kit (Ambion®,Invitrogen, CA, USA). RNA integrity and absence of DNA was confirmed by Bioanalyzer RNA Nano chips (Agilent, RIN > 9.3) and Qubit DNA High sensitivity kit, respectively. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation HT Kit following the standard protocol starting from 4 μg of total RNA using 11 cycles of PCR amplification. Sequencing was performed on 2 lanes of an Illumina HiSeq4000 (Illumina, CA, USA) multiplexing all samples. Illumina HiSeq 4000 gds 302717952 GSM2717952 GEO Accession GSM2717952 SRX3035855 GSM2717953 SRP113587 SRS2384331 GSM2717953 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from freshly dissected cerebella using Trizol (Invitrogen, CA, USA) according to the manufacturer’s instructions after homogenization by a Bullet Blender (Next Advance) and followed by isopropanol precipitation. Residual genomic DNA was removed using the Turbo DNA-free kit (Ambion®,Invitrogen, CA, USA). RNA integrity and absence of DNA was confirmed by Bioanalyzer RNA Nano chips (Agilent, RIN > 9.3) and Qubit DNA High sensitivity kit, respectively. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation HT Kit following the standard protocol starting from 4 μg of total RNA using 11 cycles of PCR amplification. Sequencing was performed on 2 lanes of an Illumina HiSeq4000 (Illumina, CA, USA) multiplexing all samples. Illumina HiSeq 4000 gds 302717953 GSM2717953 GEO Accession GSM2717953 SRX3035856 GSM2717954 SRP113587 SRS2384332 GSM2717954 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from freshly dissected cerebella using Trizol (Invitrogen, CA, USA) according to the manufacturer’s instructions after homogenization by a Bullet Blender (Next Advance) and followed by isopropanol precipitation. Residual genomic DNA was removed using the Turbo DNA-free kit (Ambion®,Invitrogen, CA, USA). RNA integrity and absence of DNA was confirmed by Bioanalyzer RNA Nano chips (Agilent, RIN > 9.3) and Qubit DNA High sensitivity kit, respectively. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation HT Kit following the standard protocol starting from 4 μg of total RNA using 11 cycles of PCR amplification. Sequencing was performed on 2 lanes of an Illumina HiSeq4000 (Illumina, CA, USA) multiplexing all samples. Illumina HiSeq 4000 gds 302717954 GSM2717954 GEO Accession GSM2717954 SRX3035857 GSM2717955 SRP113587 SRS2384333 GSM2717955 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from freshly dissected cerebella using Trizol (Invitrogen, CA, USA) according to the manufacturer’s instructions after homogenization by a Bullet Blender (Next Advance) and followed by isopropanol precipitation. Residual genomic DNA was removed using the Turbo DNA-free kit (Ambion®,Invitrogen, CA, USA). RNA integrity and absence of DNA was confirmed by Bioanalyzer RNA Nano chips (Agilent, RIN > 9.3) and Qubit DNA High sensitivity kit, respectively. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation HT Kit following the standard protocol starting from 4 μg of total RNA using 11 cycles of PCR amplification. Sequencing was performed on 2 lanes of an Illumina HiSeq4000 (Illumina, CA, USA) multiplexing all samples. Illumina HiSeq 4000 gds 302717955 GSM2717955 GEO Accession GSM2717955 SRX3035858 GSM2717956 SRP113587 SRS2384334 GSM2717956 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from freshly dissected cerebella using Trizol (Invitrogen, CA, USA) according to the manufacturer’s instructions after homogenization by a Bullet Blender (Next Advance) and followed by isopropanol precipitation. Residual genomic DNA was removed using the Turbo DNA-free kit (Ambion®,Invitrogen, CA, USA). RNA integrity and absence of DNA was confirmed by Bioanalyzer RNA Nano chips (Agilent, RIN > 9.3) and Qubit DNA High sensitivity kit, respectively. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation HT Kit following the standard protocol starting from 4 μg of total RNA using 11 cycles of PCR amplification. Sequencing was performed on 2 lanes of an Illumina HiSeq4000 (Illumina, CA, USA) multiplexing all samples. Illumina HiSeq 4000 gds 302717956 GSM2717956 GEO Accession GSM2717956 SRX3035859 GSM2717957 SRP113587 SRS2384335 GSM2717957 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from freshly dissected cerebella using Trizol (Invitrogen, CA, USA) according to the manufacturer’s instructions after homogenization by a Bullet Blender (Next Advance) and followed by isopropanol precipitation. Residual genomic DNA was removed using the Turbo DNA-free kit (Ambion®,Invitrogen, CA, USA). RNA integrity and absence of DNA was confirmed by Bioanalyzer RNA Nano chips (Agilent, RIN > 9.3) and Qubit DNA High sensitivity kit, respectively. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation HT Kit following the standard protocol starting from 4 μg of total RNA using 11 cycles of PCR amplification. Sequencing was performed on 2 lanes of an Illumina HiSeq4000 (Illumina, CA, USA) multiplexing all samples. Illumina HiSeq 4000 gds 302717957 GSM2717957 GEO Accession GSM2717957 SRX3035860 GSM2717958 SRP113587 SRS2384336 GSM2717958 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from freshly dissected cerebella using Trizol (Invitrogen, CA, USA) according to the manufacturer’s instructions after homogenization by a Bullet Blender (Next Advance) and followed by isopropanol precipitation. Residual genomic DNA was removed using the Turbo DNA-free kit (Ambion®,Invitrogen, CA, USA). RNA integrity and absence of DNA was confirmed by Bioanalyzer RNA Nano chips (Agilent, RIN > 9.3) and Qubit DNA High sensitivity kit, respectively. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation HT Kit following the standard protocol starting from 4 μg of total RNA using 11 cycles of PCR amplification. Sequencing was performed on 2 lanes of an Illumina HiSeq4000 (Illumina, CA, USA) multiplexing all samples. Illumina HiSeq 4000 gds 302717958 GSM2717958 GEO Accession GSM2717958 SRX3035861 GSM2717959 SRP113587 SRS2384337 GSM2717959 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from freshly dissected cerebella using Trizol (Invitrogen, CA, USA) according to the manufacturer’s instructions after homogenization by a Bullet Blender (Next Advance) and followed by isopropanol precipitation. Residual genomic DNA was removed using the Turbo DNA-free kit (Ambion®,Invitrogen, CA, USA). RNA integrity and absence of DNA was confirmed by Bioanalyzer RNA Nano chips (Agilent, RIN > 9.3) and Qubit DNA High sensitivity kit, respectively. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation HT Kit following the standard protocol starting from 4 μg of total RNA using 11 cycles of PCR amplification. Sequencing was performed on 2 lanes of an Illumina HiSeq4000 (Illumina, CA, USA) multiplexing all samples. Illumina HiSeq 4000 gds 302717959 GSM2717959 GEO Accession GSM2717959 SRX3035862 GSM2717960 SRP113587 SRS2384338 GSM2717960 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from freshly dissected cerebella using Trizol (Invitrogen, CA, USA) according to the manufacturer’s instructions after homogenization by a Bullet Blender (Next Advance) and followed by isopropanol precipitation. Residual genomic DNA was removed using the Turbo DNA-free kit (Ambion®,Invitrogen, CA, USA). RNA integrity and absence of DNA was confirmed by Bioanalyzer RNA Nano chips (Agilent, RIN > 9.3) and Qubit DNA High sensitivity kit, respectively. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation HT Kit following the standard protocol starting from 4 μg of total RNA using 11 cycles of PCR amplification. Sequencing was performed on 2 lanes of an Illumina HiSeq4000 (Illumina, CA, USA) multiplexing all samples. Illumina HiSeq 4000 gds 302717960 GSM2717960 GEO Accession GSM2717960 SRX3035863 GSM2717961 SRP113587 SRS2384339 GSM2717961 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from freshly dissected cerebella using Trizol (Invitrogen, CA, USA) according to the manufacturer’s instructions after homogenization by a Bullet Blender (Next Advance) and followed by isopropanol precipitation. Residual genomic DNA was removed using the Turbo DNA-free kit (Ambion®,Invitrogen, CA, USA). RNA integrity and absence of DNA was confirmed by Bioanalyzer RNA Nano chips (Agilent, RIN > 9.3) and Qubit DNA High sensitivity kit, respectively. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation HT Kit following the standard protocol starting from 4 μg of total RNA using 11 cycles of PCR amplification. Sequencing was performed on 2 lanes of an Illumina HiSeq4000 (Illumina, CA, USA) multiplexing all samples. Illumina HiSeq 4000 gds 302717961 GSM2717961 GEO Accession GSM2717961 SRX3035864 GSM2717962 SRP113587 SRS2384340 GSM2717962 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from freshly dissected cerebella using Trizol (Invitrogen, CA, USA) according to the manufacturer’s instructions after homogenization by a Bullet Blender (Next Advance) and followed by isopropanol precipitation. Residual genomic DNA was removed using the Turbo DNA-free kit (Ambion®,Invitrogen, CA, USA). RNA integrity and absence of DNA was confirmed by Bioanalyzer RNA Nano chips (Agilent, RIN > 9.3) and Qubit DNA High sensitivity kit, respectively. Sequencing libraries were prepared using the Illumina TruSeq Stranded mRNA Library Preparation HT Kit following the standard protocol starting from 4 μg of total RNA using 11 cycles of PCR amplification. Sequencing was performed on 2 lanes of an Illumina HiSeq4000 (Illumina, CA, USA) multiplexing all samples. Illumina HiSeq 4000 gds 302717962 GSM2717962 GEO Accession GSM2717962