SRX18292972 GSM6736315_r1 SRP408409 PRJNA902717 SRS15784385 GSM6736315 GSM6736315 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292973 GSM6736316_r1 SRP408409 PRJNA902717 SRS15784387 GSM6736316 GSM6736316 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292974 GSM6736317_r1 SRP408409 PRJNA902717 SRS15784386 GSM6736317 GSM6736317 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292975 GSM6736318_r1 SRP408409 PRJNA902717 SRS15784390 GSM6736318 GSM6736318 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292976 GSM6736319_r1 SRP408409 PRJNA902717 SRS15784388 GSM6736319 GSM6736319 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292977 GSM6736320_r1 SRP408409 PRJNA902717 SRS15784389 GSM6736320 GSM6736320 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292978 GSM6736321_r1 SRP408409 PRJNA902717 SRS15784391 GSM6736321 GSM6736321 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292979 GSM6736322_r1 SRP408409 PRJNA902717 SRS15784392 GSM6736322 GSM6736322 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292980 GSM6736323_r1 SRP408409 PRJNA902717 SRS15784393 GSM6736323 GSM6736323 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292981 GSM6736324_r1 SRP408409 PRJNA902717 SRS15784394 GSM6736324 GSM6736324 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292982 GSM6736325_r1 SRP408409 PRJNA902717 SRS15784395 GSM6736325 GSM6736325 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292983 GSM6736326_r1 SRP408409 PRJNA902717 SRS15784396 GSM6736326 GSM6736326 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292984 GSM6736327_r1 SRP408409 PRJNA902717 SRS15784397 GSM6736327 GSM6736327 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292985 GSM6736328_r1 SRP408409 PRJNA902717 SRS15784398 GSM6736328 GSM6736328 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292986 GSM6736329_r1 SRP408409 PRJNA902717 SRS15784399 GSM6736329 GSM6736329 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292987 GSM6736330_r1 SRP408409 PRJNA902717 SRS15784400 GSM6736330 GSM6736330 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292988 GSM6736313_r1 SRP408409 PRJNA902717 SRS15784401 GSM6736313 GSM6736313 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX18292989 GSM6736314_r1 SRP408409 PRJNA902717 SRS15784402 GSM6736314 GSM6736314 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. Bound RNA was extracted using Trizol follwing by ethanol precipitation. Small RNA-SEQ libraries containing library fragments 140-160 bp in size were generated using Illumina TruSeq small RNA adapters the protocol described in Hafner et al. (2012) Methods 58:164. RNA of 19-35 nt in length was size selected by Urea-PAGE gel extraction after adpater ligation. The final library of ~157bp was size selected on an agarose-TBE gel. Quality of final cDNA was assessed by Agilent Bioanalyzer and DNA concentration determined by Qubit. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000