SRX3203500 GSM2789655 SRP118466 SRS2529863 GSM2789655 RNA-Seq TRANSCRIPTOMIC cDNA Fluorescent cells were manually collected by using glass pipette. After washing in HBSS, collected cells were directly lysed with cell lysis buffer containing RNase inhibitor as follow manufacturer’s instruction of SMART-seq v4 (Ultra low input RNA kit, Clontech Laboratories, Inc.). After generation of cDNA from homogenous cell-type samples, the construction of library was performed by using Nextera XT DNA library prep kit (Illumina, Inc., USA) according to the manufacturer’s instructions. The double-stranded library was purified by using magnetic beads to remove all reaction components. The library was amplified to add the complete adapter sequences required for cluster generation. The finished library is purified from PCR components. Illumina HiSeq 2500 gds 302789655 GSM2789655 GEO Accession GSM2789655 SRX3203501 GSM2789656 SRP118466 SRS2529864 GSM2789656 RNA-Seq TRANSCRIPTOMIC cDNA Fluorescent cells were manually collected by using glass pipette. After washing in HBSS, collected cells were directly lysed with cell lysis buffer containing RNase inhibitor as follow manufacturer’s instruction of SMART-seq v4 (Ultra low input RNA kit, Clontech Laboratories, Inc.). After generation of cDNA from homogenous cell-type samples, the construction of library was performed by using Nextera XT DNA library prep kit (Illumina, Inc., USA) according to the manufacturer’s instructions. The double-stranded library was purified by using magnetic beads to remove all reaction components. The library was amplified to add the complete adapter sequences required for cluster generation. The finished library is purified from PCR components. Illumina HiSeq 2500 gds 302789656 GSM2789656 GEO Accession GSM2789656 SRX3203502 GSM2789657 SRP118466 SRS2529865 GSM2789657 RNA-Seq TRANSCRIPTOMIC cDNA Fluorescent cells were manually collected by using glass pipette. After washing in HBSS, collected cells were directly lysed with cell lysis buffer containing RNase inhibitor as follow manufacturer’s instruction of SMART-seq v4 (Ultra low input RNA kit, Clontech Laboratories, Inc.). After generation of cDNA from homogenous cell-type samples, the construction of library was performed by using Nextera XT DNA library prep kit (Illumina, Inc., USA) according to the manufacturer’s instructions. The double-stranded library was purified by using magnetic beads to remove all reaction components. The library was amplified to add the complete adapter sequences required for cluster generation. The finished library is purified from PCR components. Illumina HiSeq 2500 gds 302789657 GSM2789657 GEO Accession GSM2789657 SRX3203503 GSM2789658 SRP118466 SRS2529866 GSM2789658 RNA-Seq TRANSCRIPTOMIC cDNA Fluorescent cells were manually collected by using glass pipette. After washing in HBSS, collected cells were directly lysed with cell lysis buffer containing RNase inhibitor as follow manufacturer’s instruction of SMART-seq v4 (Ultra low input RNA kit, Clontech Laboratories, Inc.). After generation of cDNA from homogenous cell-type samples, the construction of library was performed by using Nextera XT DNA library prep kit (Illumina, Inc., USA) according to the manufacturer’s instructions. The double-stranded library was purified by using magnetic beads to remove all reaction components. The library was amplified to add the complete adapter sequences required for cluster generation. The finished library is purified from PCR components. Illumina HiSeq 2500 gds 302789658 GSM2789658 GEO Accession GSM2789658