SRX18465689 GSM6778124_r1 SRP411027 PRJNA907767 SRS15942289 GSM6778124 GSM6778124 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 SRX18465690 GSM6778125_r1 SRP411027 PRJNA907767 SRS15942290 GSM6778125 GSM6778125 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 SRX18465691 GSM6778126_r1 SRP411027 PRJNA907767 SRS15942291 GSM6778126 GSM6778126 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 SRX18465692 GSM6778127_r1 SRP411027 PRJNA907767 SRS15942292 GSM6778127 GSM6778127 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 SRX18465693 GSM6778128_r1 SRP411027 PRJNA907767 SRS15942293 GSM6778128 GSM6778128 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 SRX18465694 GSM6778129_r1 SRP411027 PRJNA907767 SRS15942294 GSM6778129 GSM6778129 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 SRX18465695 GSM6778130_r1 SRP411027 PRJNA907767 SRS15942295 GSM6778130 GSM6778130 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 SRX18465696 GSM6778131_r1 SRP411027 PRJNA907767 SRS15942296 GSM6778131 GSM6778131 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