SRX5168420 GSM3523224 SRP174004 SRS4176864 GSM3523224 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish brains from Tg(her4.1:EGFP) were dissected after PBS or IL4 injections at 24 hpi. Cells were dissociated with Miltenyi Neural Tissue Dissociation Kit as described (Kyritsis et al., 2012). Cells were sorted with BD Aria II FACS machine, RNA was isolated using Norgen Total RNA Purification Kit. Complete cDNA was synthesized from the obtained mRNA with SmartScribe reverse transcriptase using a universally tailed poly-dT primer and template switching oligo. This was followed by amplification of the purified cDNA with the Advantage 2 DNA Polymerase. After ultrasonic shearing of the amplified cDNA (Covaris S2) samples were subjected to standard Illumina fragment library preparation using the NEBnext chemistries (New England Biolabs). Libraries were purified using XP beads (Beckman Coulter), quantified by qPCR (KAPA Biosysytems) and subjected to Illumina 75bp single-end sequencing on the Illumina HiSeq2000 platform providing on average 31 million reads per sample. Illumina HiSeq 2000 gds 303523224 GSM3523224 GEO Accession GSM3523224 SRX5168421 GSM3523225 SRP174004 SRS4176866 GSM3523225 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish brains from Tg(her4.1:EGFP) were dissected after PBS or IL4 injections at 24 hpi. Cells were dissociated with Miltenyi Neural Tissue Dissociation Kit as described (Kyritsis et al., 2012). Cells were sorted with BD Aria II FACS machine, RNA was isolated using Norgen Total RNA Purification Kit. Complete cDNA was synthesized from the obtained mRNA with SmartScribe reverse transcriptase using a universally tailed poly-dT primer and template switching oligo. This was followed by amplification of the purified cDNA with the Advantage 2 DNA Polymerase. After ultrasonic shearing of the amplified cDNA (Covaris S2) samples were subjected to standard Illumina fragment library preparation using the NEBnext chemistries (New England Biolabs). Libraries were purified using XP beads (Beckman Coulter), quantified by qPCR (KAPA Biosysytems) and subjected to Illumina 75bp single-end sequencing on the Illumina HiSeq2000 platform providing on average 31 million reads per sample. Illumina HiSeq 2000 gds 303523225 GSM3523225 GEO Accession GSM3523225 SRX5168422 GSM3523226 SRP174004 SRS4176867 GSM3523226 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish brains from Tg(her4.1:EGFP) were dissected after PBS or IL4 injections at 24 hpi. Cells were dissociated with Miltenyi Neural Tissue Dissociation Kit as described (Kyritsis et al., 2012). Cells were sorted with BD Aria II FACS machine, RNA was isolated using Norgen Total RNA Purification Kit. Complete cDNA was synthesized from the obtained mRNA with SmartScribe reverse transcriptase using a universally tailed poly-dT primer and template switching oligo. This was followed by amplification of the purified cDNA with the Advantage 2 DNA Polymerase. After ultrasonic shearing of the amplified cDNA (Covaris S2) samples were subjected to standard Illumina fragment library preparation using the NEBnext chemistries (New England Biolabs). Libraries were purified using XP beads (Beckman Coulter), quantified by qPCR (KAPA Biosysytems) and subjected to Illumina 75bp single-end sequencing on the Illumina HiSeq2000 platform providing on average 31 million reads per sample. Illumina HiSeq 2000 gds 303523226 GSM3523226 GEO Accession GSM3523226 SRX5168423 GSM3523227 SRP174004 SRS4176865 GSM3523227 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish brains from Tg(her4.1:EGFP) were dissected after PBS or IL4 injections at 24 hpi. Cells were dissociated with Miltenyi Neural Tissue Dissociation Kit as described (Kyritsis et al., 2012). Cells were sorted with BD Aria II FACS machine, RNA was isolated using Norgen Total RNA Purification Kit. Complete cDNA was synthesized from the obtained mRNA with SmartScribe reverse transcriptase using a universally tailed poly-dT primer and template switching oligo. This was followed by amplification of the purified cDNA with the Advantage 2 DNA Polymerase. After ultrasonic shearing of the amplified cDNA (Covaris S2) samples were subjected to standard Illumina fragment library preparation using the NEBnext chemistries (New England Biolabs). Libraries were purified using XP beads (Beckman Coulter), quantified by qPCR (KAPA Biosysytems) and subjected to Illumina 75bp single-end sequencing on the Illumina HiSeq2000 platform providing on average 31 million reads per sample. Illumina HiSeq 2000 gds 303523227 GSM3523227 GEO Accession GSM3523227 SRX5168424 GSM3523228 SRP174004 SRS4176868 GSM3523228 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish brains from Tg(her4.1:EGFP) were dissected after PBS or IL4 injections at 24 hpi. Cells were dissociated with Miltenyi Neural Tissue Dissociation Kit as described (Kyritsis et al., 2012). Cells were sorted with BD Aria II FACS machine, RNA was isolated using Norgen Total RNA Purification Kit. Complete cDNA was synthesized from the obtained mRNA with SmartScribe reverse transcriptase using a universally tailed poly-dT primer and template switching oligo. This was followed by amplification of the purified cDNA with the Advantage 2 DNA Polymerase. After ultrasonic shearing of the amplified cDNA (Covaris S2) samples were subjected to standard Illumina fragment library preparation using the NEBnext chemistries (New England Biolabs). Libraries were purified using XP beads (Beckman Coulter), quantified by qPCR (KAPA Biosysytems) and subjected to Illumina 75bp single-end sequencing on the Illumina HiSeq2000 platform providing on average 31 million reads per sample. Illumina HiSeq 2000 gds 303523228 GSM3523228 GEO Accession GSM3523228 SRX5168425 GSM3523229 SRP174004 SRS4176869 GSM3523229 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish brains from Tg(her4.1:EGFP) were dissected after PBS or IL4 injections at 24 hpi. Cells were dissociated with Miltenyi Neural Tissue Dissociation Kit as described (Kyritsis et al., 2012). Cells were sorted with BD Aria II FACS machine, RNA was isolated using Norgen Total RNA Purification Kit. Complete cDNA was synthesized from the obtained mRNA with SmartScribe reverse transcriptase using a universally tailed poly-dT primer and template switching oligo. This was followed by amplification of the purified cDNA with the Advantage 2 DNA Polymerase. After ultrasonic shearing of the amplified cDNA (Covaris S2) samples were subjected to standard Illumina fragment library preparation using the NEBnext chemistries (New England Biolabs). Libraries were purified using XP beads (Beckman Coulter), quantified by qPCR (KAPA Biosysytems) and subjected to Illumina 75bp single-end sequencing on the Illumina HiSeq2000 platform providing on average 31 million reads per sample. Illumina HiSeq 2000 gds 303523229 GSM3523229 GEO Accession GSM3523229 SRX5168426 GSM3523230 SRP174004 SRS4176870 GSM3523230 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish brains from Tg(her4.1:EGFP) were dissected after PBS or IL4 injections at 24 hpi. Cells were dissociated with Miltenyi Neural Tissue Dissociation Kit as described (Kyritsis et al., 2012). Cells were sorted with BD Aria II FACS machine, RNA was isolated using Norgen Total RNA Purification Kit. Complete cDNA was synthesized from the obtained mRNA with SmartScribe reverse transcriptase using a universally tailed poly-dT primer and template switching oligo. This was followed by amplification of the purified cDNA with the Advantage 2 DNA Polymerase. After ultrasonic shearing of the amplified cDNA (Covaris S2) samples were subjected to standard Illumina fragment library preparation using the NEBnext chemistries (New England Biolabs). Libraries were purified using XP beads (Beckman Coulter), quantified by qPCR (KAPA Biosysytems) and subjected to Illumina 75bp single-end sequencing on the Illumina HiSeq2000 platform providing on average 31 million reads per sample. Illumina HiSeq 2000 gds 303523230 GSM3523230 GEO Accession GSM3523230 SRX5168427 GSM3523231 SRP174004 SRS4176871 GSM3523231 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish brains from Tg(her4.1:EGFP) were dissected after PBS or IL4 injections at 24 hpi. Cells were dissociated with Miltenyi Neural Tissue Dissociation Kit as described (Kyritsis et al., 2012). Cells were sorted with BD Aria II FACS machine, RNA was isolated using Norgen Total RNA Purification Kit. Complete cDNA was synthesized from the obtained mRNA with SmartScribe reverse transcriptase using a universally tailed poly-dT primer and template switching oligo. This was followed by amplification of the purified cDNA with the Advantage 2 DNA Polymerase. After ultrasonic shearing of the amplified cDNA (Covaris S2) samples were subjected to standard Illumina fragment library preparation using the NEBnext chemistries (New England Biolabs). Libraries were purified using XP beads (Beckman Coulter), quantified by qPCR (KAPA Biosysytems) and subjected to Illumina 75bp single-end sequencing on the Illumina HiSeq2000 platform providing on average 31 million reads per sample. Illumina HiSeq 2000 gds 303523231 GSM3523231 GEO Accession GSM3523231