SRX5103048 GSM3504506 SRP172787 SRS4113209 GSM3504506 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504506 GSM3504506 GEO Accession GSM3504506 SRX5103049 GSM3504507 SRP172787 SRS4113211 GSM3504507 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504507 GSM3504507 GEO Accession GSM3504507 SRX5103050 GSM3504508 SRP172787 SRS4113210 GSM3504508 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504508 GSM3504508 GEO Accession GSM3504508 SRX5103051 GSM3504509 SRP172787 SRS4113212 GSM3504509 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504509 GSM3504509 GEO Accession GSM3504509 SRX5103052 GSM3504510 SRP172787 SRS4113213 GSM3504510 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504510 GSM3504510 GEO Accession GSM3504510 SRX5103053 GSM3504511 SRP172787 SRS4113215 GSM3504511 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504511 GSM3504511 GEO Accession GSM3504511 SRX5103054 GSM3504512 SRP172787 SRS4113214 GSM3504512 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504512 GSM3504512 GEO Accession GSM3504512 SRX5103055 GSM3504513 SRP172787 SRS4113216 GSM3504513 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504513 GSM3504513 GEO Accession GSM3504513 SRX5103056 GSM3504514 SRP172787 SRS4113217 GSM3504514 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504514 GSM3504514 GEO Accession GSM3504514 SRX5103057 GSM3504515 SRP172787 SRS4113218 GSM3504515 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504515 GSM3504515 GEO Accession GSM3504515 SRX5103058 GSM3504516 SRP172787 SRS4113219 GSM3504516 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504516 GSM3504516 GEO Accession GSM3504516 SRX5103059 GSM3504517 SRP172787 SRS4113220 GSM3504517 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504517 GSM3504517 GEO Accession GSM3504517 SRX5103060 GSM3504518 SRP172787 SRS4113221 GSM3504518 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504518 GSM3504518 GEO Accession GSM3504518 SRX5103061 GSM3504519 SRP172787 SRS4113222 GSM3504519 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504519 GSM3504519 GEO Accession GSM3504519 SRX5103062 GSM3504520 SRP172787 SRS4113223 GSM3504520 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504520 GSM3504520 GEO Accession GSM3504520 SRX5103063 GSM3504521 SRP172787 SRS4113224 GSM3504521 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504521 GSM3504521 GEO Accession GSM3504521 SRX5103064 GSM3504522 SRP172787 SRS4113225 GSM3504522 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504522 GSM3504522 GEO Accession GSM3504522 SRX5103065 GSM3504523 SRP172787 SRS4113226 GSM3504523 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504523 GSM3504523 GEO Accession GSM3504523 SRX5103066 GSM3504524 SRP172787 SRS4113227 GSM3504524 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504524 GSM3504524 GEO Accession GSM3504524 SRX5103067 GSM3504525 SRP172787 SRS4113228 GSM3504525 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504525 GSM3504525 GEO Accession GSM3504525 SRX5103068 GSM3504526 SRP172787 SRS4113229 GSM3504526 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504526 GSM3504526 GEO Accession GSM3504526 SRX5103069 GSM3504527 SRP172787 SRS4113231 GSM3504527 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504527 GSM3504527 GEO Accession GSM3504527 SRX5103070 GSM3504528 SRP172787 SRS4113230 GSM3504528 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504528 GSM3504528 GEO Accession GSM3504528 SRX5103071 GSM3504529 SRP172787 SRS4113232 GSM3504529 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504529 GSM3504529 GEO Accession GSM3504529 SRX5103072 GSM3504530 SRP172787 SRS4113233 GSM3504530 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504530 GSM3504530 GEO Accession GSM3504530 SRX5103073 GSM3504531 SRP172787 SRS4113234 GSM3504531 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504531 GSM3504531 GEO Accession GSM3504531 SRX5103074 GSM3504532 SRP172787 SRS4113235 GSM3504532 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504532 GSM3504532 GEO Accession GSM3504532 SRX5103075 GSM3504533 SRP172787 SRS4113236 GSM3504533 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504533 GSM3504533 GEO Accession GSM3504533 SRX5103076 GSM3504534 SRP172787 SRS4113237 GSM3504534 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504534 GSM3504534 GEO Accession GSM3504534 SRX5103077 GSM3504535 SRP172787 SRS4113239 GSM3504535 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504535 GSM3504535 GEO Accession GSM3504535 SRX5103078 GSM3504536 SRP172787 SRS4113238 GSM3504536 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504536 GSM3504536 GEO Accession GSM3504536 SRX5103079 GSM3504537 SRP172787 SRS4113240 GSM3504537 RNA-Seq TRANSCRIPTOMIC cDNA Microglia were isolated using CD11b MicroBeads methods. Total RNA were isolated and sent to Cofactor Genomics (St. Louis, USA) for RNA deep sequencing. RNA samples were first examined using Agilent Bioanalyzer (Agilent Technologies, Palo Alto, CA, USA) for purity and quality. RNAs were reverse transcribed to cDNA using Ovation RNA-Seq System Version 2 (NuGEN, San Carlos, CA) according to the manufacturer's protocol. The resulting cDNAs were then sheared using a focused ultrasonicator (Covaris Inc., Woburn, MA, USA) and the libraries were prepared using the Kapa LTP Library Preparation Kit (Illumina, San Diego, CA, USA) Illumina HiSeq 2000 gds 303504537 GSM3504537 GEO Accession GSM3504537