SRX15015096 GSM6069564_r1 SRP372507 PRJNA832695 SRS12763526 GSM6069564 GSM6069564 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cells were subjected to pull down with a GW182 peptide bound to anti-FLAG M2 Magnetic beads RNA at a size of 19-35 nt was gel extracted and used to generate library The quality and quantity of the RNA samples was checked using an Agilent bio-analyzer. Small RNA-SEQ libraries were generated using Illumina small RNA SEQ kits using the Illumina provided protocol containing library fragments 140-160 bp in size. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX15015097 GSM6069565_r1 SRP372507 PRJNA832695 SRS12764210 GSM6069565 GSM6069565 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cells were subjected to pull down with a GW182 peptide bound to anti-FLAG M2 Magnetic beads RNA at a size of 19-35 nt was gel extracted and used to generate library The quality and quantity of the RNA samples was checked using an Agilent bio-analyzer. Small RNA-SEQ libraries were generated using Illumina small RNA SEQ kits using the Illumina provided protocol containing library fragments 140-160 bp in size. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX15015098 GSM6069566_r1 SRP372507 PRJNA832695 SRS12763963 GSM6069566 GSM6069566 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cells were subjected to pull down with a GW182 peptide bound to anti-FLAG M2 Magnetic beads RNA at a size of 19-35 nt was gel extracted and used to generate library The quality and quantity of the RNA samples was checked using an Agilent bio-analyzer. Small RNA-SEQ libraries were generated using Illumina small RNA SEQ kits using the Illumina provided protocol containing library fragments 140-160 bp in size. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX15015099 GSM6069567_r1 SRP372507 PRJNA832695 SRS12763527 GSM6069567 GSM6069567 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cells were subjected to pull down with a GW182 peptide bound to anti-FLAG M2 Magnetic beads RNA at a size of 19-35 nt was gel extracted and used to generate library The quality and quantity of the RNA samples was checked using an Agilent bio-analyzer. Small RNA-SEQ libraries were generated using Illumina small RNA SEQ kits using the Illumina provided protocol containing library fragments 140-160 bp in size. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX15015100 GSM6069568_r1 SRP372507 PRJNA832695 SRS12764966 GSM6069568 GSM6069568 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cells were subjected to pull down with a GW182 peptide bound to anti-FLAG M2 Magnetic beads RNA at a size of 19-35 nt was gel extracted and used to generate library The quality and quantity of the RNA samples was checked using an Agilent bio-analyzer. Small RNA-SEQ libraries were generated using Illumina small RNA SEQ kits using the Illumina provided protocol containing library fragments 140-160 bp in size. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX15015101 GSM6069569_r1 SRP372507 PRJNA832695 SRS12763528 GSM6069569 GSM6069569 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cells were subjected to pull down with a GW182 peptide bound to anti-FLAG M2 Magnetic beads RNA at a size of 19-35 nt was gel extracted and used to generate library The quality and quantity of the RNA samples was checked using an Agilent bio-analyzer. Small RNA-SEQ libraries were generated using Illumina small RNA SEQ kits using the Illumina provided protocol containing library fragments 140-160 bp in size. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX15015102 GSM6069570_r1 SRP372507 PRJNA832695 SRS12763529 GSM6069570 GSM6069570 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cells were subjected to pull down with a GW182 peptide bound to anti-FLAG M2 Magnetic beads RNA at a size of 19-35 nt was gel extracted and used to generate library The quality and quantity of the RNA samples was checked using an Agilent bio-analyzer. Small RNA-SEQ libraries were generated using Illumina small RNA SEQ kits using the Illumina provided protocol containing library fragments 140-160 bp in size. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX15015103 GSM6069571_r1 SRP372507 PRJNA832695 SRS12763964 GSM6069571 GSM6069571 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cells were subjected to pull down with a GW182 peptide bound to anti-FLAG M2 Magnetic beads RNA at a size of 19-35 nt was gel extracted and used to generate library The quality and quantity of the RNA samples was checked using an Agilent bio-analyzer. Small RNA-SEQ libraries were generated using Illumina small RNA SEQ kits using the Illumina provided protocol containing library fragments 140-160 bp in size. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX15015104 GSM6069572_r1 SRP372507 PRJNA832695 SRS12763530 GSM6069572 GSM6069572 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cells were subjected to pull down with a GW182 peptide bound to anti-FLAG M2 Magnetic beads RNA at a size of 19-35 nt was gel extracted and used to generate library The quality and quantity of the RNA samples was checked using an Agilent bio-analyzer. Small RNA-SEQ libraries were generated using Illumina small RNA SEQ kits using the Illumina provided protocol containing library fragments 140-160 bp in size. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000 SRX15015105 GSM6069573_r1 SRP372507 PRJNA832695 SRS12763531 GSM6069573 GSM6069573 ncRNA-Seq TRANSCRIPTOMIC size fractionation Cells were subjected to pull down with a GW182 peptide bound to anti-FLAG M2 Magnetic beads RNA at a size of 19-35 nt was gel extracted and used to generate library The quality and quantity of the RNA samples was checked using an Agilent bio-analyzer. Small RNA-SEQ libraries were generated using Illumina small RNA SEQ kits using the Illumina provided protocol containing library fragments 140-160 bp in size. RNA-Seq; sequenced on an Illumina HiSEQ4000 using Illumina provided reagents and protocols Illumina HiSeq 4000