SRX18465671 GSM6778096_r1 SRP411025 PRJNA907763 SRS15942271 GSM6778096 GSM6778096 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cell lysates were subjected to pull down with a GW182 FLAG-GST-T6B peptide isolated using anti-FLAG M2 Magnetic beads. RNA was extracted using Trizol followed by an ethanol precipitation. Small RNA-Seq libraries were generated using illumina TruSeq small RNA adapters. RNA 19-35 nucleotides were size selected by Urea-PAGE gel extraction after each round of adapter ligation. The final library ~156 bp was size selected on an agarose-TBE gel. Final cDNA quality was assessed by Agilent Bioanalyzer and DNA concetration was determined by Qubit. Illumina HiSeq 4000 SRX18465672 GSM6778097_r1 SRP411025 PRJNA907763 SRS15942272 GSM6778097 GSM6778097 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cell lysates were subjected to pull down with a GW182 FLAG-GST-T6B peptide isolated using anti-FLAG M2 Magnetic beads. RNA was extracted using Trizol followed by an ethanol precipitation. Small RNA-Seq libraries were generated using illumina TruSeq small RNA adapters. RNA 19-35 nucleotides were size selected by Urea-PAGE gel extraction after each round of adapter ligation. The final library ~156 bp was size selected on an agarose-TBE gel. Final cDNA quality was assessed by Agilent Bioanalyzer and DNA concetration was determined by Qubit. Illumina HiSeq 4000 SRX18465673 GSM6778098_r1 SRP411025 PRJNA907763 SRS15942273 GSM6778098 GSM6778098 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cell lysates were subjected to pull down with a GW182 FLAG-GST-T6B peptide isolated using anti-FLAG M2 Magnetic beads. RNA was extracted using Trizol followed by an ethanol precipitation. Small RNA-Seq libraries were generated using illumina TruSeq small RNA adapters. RNA 19-35 nucleotides were size selected by Urea-PAGE gel extraction after each round of adapter ligation. The final library ~156 bp was size selected on an agarose-TBE gel. Final cDNA quality was assessed by Agilent Bioanalyzer and DNA concetration was determined by Qubit. Illumina HiSeq 4000 SRX18465674 GSM6778099_r1 SRP411025 PRJNA907763 SRS15942274 GSM6778099 GSM6778099 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cell lysates were subjected to pull down with a GW182 FLAG-GST-T6B peptide isolated using anti-FLAG M2 Magnetic beads. RNA was extracted using Trizol followed by an ethanol precipitation. Small RNA-Seq libraries were generated using illumina TruSeq small RNA adapters. RNA 19-35 nucleotides were size selected by Urea-PAGE gel extraction after each round of adapter ligation. The final library ~156 bp was size selected on an agarose-TBE gel. Final cDNA quality was assessed by Agilent Bioanalyzer and DNA concetration was determined by Qubit. Illumina HiSeq 4000 SRX18465675 GSM6778100_r1 SRP411025 PRJNA907763 SRS15942275 GSM6778100 GSM6778100 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cell lysates were subjected to pull down with a GW182 FLAG-GST-T6B peptide isolated using anti-FLAG M2 Magnetic beads. RNA was extracted using Trizol followed by an ethanol precipitation. Small RNA-Seq libraries were generated using illumina TruSeq small RNA adapters. RNA 19-35 nucleotides were size selected by Urea-PAGE gel extraction after each round of adapter ligation. The final library ~156 bp was size selected on an agarose-TBE gel. Final cDNA quality was assessed by Agilent Bioanalyzer and DNA concetration was determined by Qubit. Illumina HiSeq 4000 SRX18465676 GSM6778101_r1 SRP411025 PRJNA907763 SRS15942276 GSM6778101 GSM6778101 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cell lysates were subjected to pull down with a GW182 FLAG-GST-T6B peptide isolated using anti-FLAG M2 Magnetic beads. RNA was extracted using Trizol followed by an ethanol precipitation. Small RNA-Seq libraries were generated using illumina TruSeq small RNA adapters. RNA 19-35 nucleotides were size selected by Urea-PAGE gel extraction after each round of adapter ligation. The final library ~156 bp was size selected on an agarose-TBE gel. Final cDNA quality was assessed by Agilent Bioanalyzer and DNA concetration was determined by Qubit. Illumina HiSeq 4000