SRX15209851 GSM6123698_r1 SRP374309 PRJNA836500 SRS12948372 GSM6123698 GSM6123698 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209852 GSM6123699_r1 SRP374309 PRJNA836500 SRS12948373 GSM6123699 GSM6123699 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209853 GSM6123700_r1 SRP374309 PRJNA836500 SRS12948374 GSM6123700 GSM6123700 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209854 GSM6123701_r1 SRP374309 PRJNA836500 SRS12948375 GSM6123701 GSM6123701 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209855 GSM6123702_r1 SRP374309 PRJNA836500 SRS12948376 GSM6123702 GSM6123702 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209856 GSM6123703_r1 SRP374309 PRJNA836500 SRS12948377 GSM6123703 GSM6123703 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209857 GSM6123704_r1 SRP374309 PRJNA836500 SRS12948378 GSM6123704 GSM6123704 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209858 GSM6123705_r1 SRP374309 PRJNA836500 SRS12948379 GSM6123705 GSM6123705 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209859 GSM6123706_r1 SRP374309 PRJNA836500 SRS12948380 GSM6123706 GSM6123706 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209860 GSM6123707_r1 SRP374309 PRJNA836500 SRS12948381 GSM6123707 GSM6123707 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209861 GSM6123708_r1 SRP374309 PRJNA836500 SRS12948382 GSM6123708 GSM6123708 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209862 GSM6123709_r1 SRP374309 PRJNA836500 SRS12948383 GSM6123709 GSM6123709 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209863 GSM6123710_r1 SRP374309 PRJNA836500 SRS12948384 GSM6123710 GSM6123710 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209864 GSM6123711_r1 SRP374309 PRJNA836500 SRS12948385 GSM6123711 GSM6123711 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209865 GSM6123712_r1 SRP374309 PRJNA836500 SRS12948386 GSM6123712 GSM6123712 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209866 GSM6123695_r1 SRP374309 PRJNA836500 SRS12948387 GSM6123695 GSM6123695 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209867 GSM6123696_r1 SRP374309 PRJNA836500 SRS12948388 GSM6123696 GSM6123696 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000 SRX15209868 GSM6123697_r1 SRP374309 PRJNA836500 SRS12948389 GSM6123697 GSM6123697 miRNA-Seq TRANSCRIPTOMIC size fractionation Gel purification The input and uncleaved pre-miRNAs were subjected to AQ-seq as previously described (Kim et al., 2019), with some modifications as follows. After 3′ adapter ligation, the ligated RNAs were purified on a 10% urea-polyacrylamide gel along with Century-Plus RNA Markers (Thermo Fisher) as a size marker. After reverse transcription, cDNAs were amplified with NEBNext Ultra II Q5 Master Mix (NEB). The libraries were sequenced on the NovaSeq 6000 platform. Illumina NovaSeq 6000