SRX23483066 GSM8056728_r1 SRP487218 PRJNA1071589 SRS20335498 GSM8056728 GSM8056728 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483067 GSM8056729_r1 SRP487218 PRJNA1071589 SRS20335499 GSM8056729 GSM8056729 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483068 GSM8056730_r1 SRP487218 PRJNA1071589 SRS20335500 GSM8056730 GSM8056730 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483069 GSM8056731_r1 SRP487218 PRJNA1071589 SRS20335502 GSM8056731 GSM8056731 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483070 GSM8056732_r1 SRP487218 PRJNA1071589 SRS20335501 GSM8056732 GSM8056732 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483071 GSM8056733_r1 SRP487218 PRJNA1071589 SRS20335503 GSM8056733 GSM8056733 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483072 GSM8056734_r1 SRP487218 PRJNA1071589 SRS20335504 GSM8056734 GSM8056734 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483073 GSM8056735_r1 SRP487218 PRJNA1071589 SRS20335505 GSM8056735 GSM8056735 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483074 GSM8056736_r1 SRP487218 PRJNA1071589 SRS20335509 GSM8056736 GSM8056736 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483075 GSM8056737_r1 SRP487218 PRJNA1071589 SRS20335506 GSM8056737 GSM8056737 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483076 GSM8056738_r1 SRP487218 PRJNA1071589 SRS20335508 GSM8056738 GSM8056738 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483077 GSM8056739_r1 SRP487218 PRJNA1071589 SRS20335507 GSM8056739 GSM8056739 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483078 GSM8056740_r1 SRP487218 PRJNA1071589 SRS20335511 GSM8056740 GSM8056740 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483079 GSM8056741_r1 SRP487218 PRJNA1071589 SRS20335510 GSM8056741 GSM8056741 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483080 GSM8056742_r1 SRP487218 PRJNA1071589 SRS20335512 GSM8056742 GSM8056742 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483081 GSM8056743_r1 SRP487218 PRJNA1071589 SRS20335514 GSM8056743 GSM8056743 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483082 GSM8056744_r1 SRP487218 PRJNA1071589 SRS20335513 GSM8056744 GSM8056744 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483083 GSM8056745_r1 SRP487218 PRJNA1071589 SRS20335515 GSM8056745 GSM8056745 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483084 GSM8056746_r1 SRP487218 PRJNA1071589 SRS20335516 GSM8056746 GSM8056746 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483085 GSM8056747_r1 SRP487218 PRJNA1071589 SRS20335517 GSM8056747 GSM8056747 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483086 GSM8056748_r1 SRP487218 PRJNA1071589 SRS20335519 GSM8056748 GSM8056748 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483087 GSM8056749_r1 SRP487218 PRJNA1071589 SRS20335518 GSM8056749 GSM8056749 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483088 GSM8056750_r1 SRP487218 PRJNA1071589 SRS20335521 GSM8056750 GSM8056750 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq SRX23483089 GSM8056751_r1 SRP487218 PRJNA1071589 SRS20335520 GSM8056751 GSM8056751 OTHER TRANSCRIPTOMIC other RNA was then extracted from washed beads using Trizol LS and treated with T4 Polynucleotide Kinase to obtain 5' phosphate ends for subsequent ligations and passed through NucAway columns to remove RNAs <20 nt in length. Small RNA libraries were generated using NEBNext Multiplex Small RNA Library Prep following the manufacturer's recommendations for 100ng input material. PCR-amplified small RNA libraries were size selected to 130-200 bp fragments. Libraries characterized on an Agilent Tape Station on a DNA1000 High-Sensitivity Screen Tape and quantified by Qubit were pooled and sequenced at 75 bp read length on the MiSeq platform Illumina MiSeq