SRX12419801 GSM5606884_r1 SRP339575 PRJNA767701 SRS10387378 GSM5606884 GSM5606884 ncRNA-Seq TRANSCRIPTOMIC size fractionation RNA was isolated from 100 µL of P100 pellet using a PicoPure RNA isolation kit (ThermoFisher). The RNA (1-3 µg) was then treated with 5 units of RNase R (Lucigen. RNR07250) for one hour at 37°C. RNA-seq libraries were generated using the NEBNext® Ultra™ II Directional RNA Library Prep Kit for Illumina® (catalog number E7765; New England Biolabs) using 500 ng of total RNA as starting material. RNA-seq libraries were sequenced using paired-end 300-bp reads. Sequencing was performed at the Center for Genomics and Bioinformatics at Indiana University, Bloomington (IN, USA). NextSeq 550 SRX12419802 GSM5606885_r1 SRP339575 PRJNA767701 SRS10387379 GSM5606885 GSM5606885 ncRNA-Seq TRANSCRIPTOMIC size fractionation RNA was isolated from 100 µL of P100 pellet using a PicoPure RNA isolation kit (ThermoFisher). The RNA (1-3 µg) was then treated with 5 units of RNase R (Lucigen. RNR07250) for one hour at 37°C. RNA-seq libraries were generated using the NEBNext® Ultra™ II Directional RNA Library Prep Kit for Illumina® (catalog number E7765; New England Biolabs) using 500 ng of total RNA as starting material. RNA-seq libraries were sequenced using paired-end 300-bp reads. Sequencing was performed at the Center for Genomics and Bioinformatics at Indiana University, Bloomington (IN, USA). NextSeq 550 SRX12419803 GSM5606886_r1 SRP339575 PRJNA767701 SRS10387381 GSM5606886 GSM5606886 ncRNA-Seq TRANSCRIPTOMIC size fractionation RNA was isolated from 100 µL of P100 pellet using a PicoPure RNA isolation kit (ThermoFisher). The RNA (1-3 µg) was then treated with 5 units of RNase R (Lucigen. RNR07250) for one hour at 37°C. RNA-seq libraries were generated using the NEBNext® Ultra™ II Directional RNA Library Prep Kit for Illumina® (catalog number E7765; New England Biolabs) using 500 ng of total RNA as starting material. RNA-seq libraries were sequenced using paired-end 300-bp reads. Sequencing was performed at the Center for Genomics and Bioinformatics at Indiana University, Bloomington (IN, USA). NextSeq 550 SRX12419804 GSM5606887_r1 SRP339575 PRJNA767701 SRS10387383 GSM5606887 GSM5606887 ncRNA-Seq TRANSCRIPTOMIC size fractionation RNA was isolated from 100 µL of P100 pellet using a PicoPure RNA isolation kit (ThermoFisher). The RNA (1-3 µg) was then treated with 5 units of RNase R (Lucigen. RNR07250) for one hour at 37°C. RNA-seq libraries were generated using the NEBNext® Ultra™ II Directional RNA Library Prep Kit for Illumina® (catalog number E7765; New England Biolabs) using 500 ng of total RNA as starting material. RNA-seq libraries were sequenced using paired-end 300-bp reads. Sequencing was performed at the Center for Genomics and Bioinformatics at Indiana University, Bloomington (IN, USA). NextSeq 550 SRX12419805 GSM5606888_r1 SRP339575 PRJNA767701 SRS10387380 GSM5606888 GSM5606888 ncRNA-Seq TRANSCRIPTOMIC size fractionation RNA was isolated from 100 µL of P100 pellet using a PicoPure RNA isolation kit (ThermoFisher). The RNA (1-3 µg) was then treated with 5 units of RNase R (Lucigen. RNR07250) for one hour at 37°C. RNA-seq libraries were generated using the NEBNext® Ultra™ II Directional RNA Library Prep Kit for Illumina® (catalog number E7765; New England Biolabs) using 500 ng of total RNA as starting material. RNA-seq libraries were sequenced using paired-end 300-bp reads. Sequencing was performed at the Center for Genomics and Bioinformatics at Indiana University, Bloomington (IN, USA). NextSeq 550 SRX12419806 GSM5606889_r1 SRP339575 PRJNA767701 SRS10387382 GSM5606889 GSM5606889 ncRNA-Seq TRANSCRIPTOMIC size fractionation RNA was isolated from 100 µL of P100 pellet using a PicoPure RNA isolation kit (ThermoFisher). The RNA (1-3 µg) was then treated with 5 units of RNase R (Lucigen. RNR07250) for one hour at 37°C. RNA-seq libraries were generated using the NEBNext® Ultra™ II Directional RNA Library Prep Kit for Illumina® (catalog number E7765; New England Biolabs) using 500 ng of total RNA as starting material. RNA-seq libraries were sequenced using paired-end 300-bp reads. Sequencing was performed at the Center for Genomics and Bioinformatics at Indiana University, Bloomington (IN, USA). NextSeq 550