SRX5619073 GSM3700965 SRP190019 SRS4571377 GSM3700965 OTHER TRANSCRIPTOMIC other Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 40-80 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303700965 GSM3700965 GEO Accession GSM3700965 SRX5619074 GSM3700966 SRP190019 SRS4571375 GSM3700966 OTHER TRANSCRIPTOMIC other Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 40-80 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303700966 GSM3700966 GEO Accession GSM3700966 SRX5619075 GSM3700967 SRP190019 SRS4571376 GSM3700967 OTHER TRANSCRIPTOMIC other Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 40-80 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303700967 GSM3700967 GEO Accession GSM3700967 SRX5619077 GSM3700969 SRP190019 SRS4571380 GSM3700969 OTHER TRANSCRIPTOMIC other Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 40-80 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303700969 GSM3700969 GEO Accession GSM3700969 SRX5619078 GSM3700970 SRP190019 SRS4571381 GSM3700970 OTHER TRANSCRIPTOMIC other Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 40-80 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303700970 GSM3700970 GEO Accession GSM3700970 SRX5619079 GSM3700971 SRP190019 SRS4571379 GSM3700971 OTHER TRANSCRIPTOMIC other Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 40-80 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303700971 GSM3700971 GEO Accession GSM3700971 SRX5619080 GSM3700972 SRP190019 SRS4571378 GSM3700972 OTHER TRANSCRIPTOMIC other Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 40-80 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303700972 GSM3700972 GEO Accession GSM3700972 SRX5619081 GSM3700973 SRP190019 SRS4571383 GSM3700973 OTHER TRANSCRIPTOMIC other Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 40-80 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303700973 GSM3700973 GEO Accession GSM3700973 SRX5619082 GSM3700974 SRP190019 SRS4571384 GSM3700974 OTHER TRANSCRIPTOMIC other Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 40-80 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303700974 GSM3700974 GEO Accession GSM3700974 SRX5619083 GSM3700975 SRP190019 SRS4571385 GSM3700975 OTHER TRANSCRIPTOMIC other Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 40-80 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303700975 GSM3700975 GEO Accession GSM3700975 SRX5619084 GSM3700976 SRP190019 SRS4571386 GSM3700976 OTHER TRANSCRIPTOMIC other Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 40-80 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303700976 GSM3700976 GEO Accession GSM3700976 SRX6077640 GSM3893141 SRP190019 PRJNA530200 SRS4979449 GSM3893141 RNA-Seq TRANSCRIPTOMIC cDNA Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 15-90 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303893141 GSM3893141 GEO Accession GSM3893141 SRX6077641 GSM3893142 SRP190019 PRJNA530200 SRS4979450 GSM3893142 RNA-Seq TRANSCRIPTOMIC cDNA Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 15-90 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303893142 GSM3893142 GEO Accession GSM3893142 SRX6077642 GSM3893143 SRP190019 PRJNA530200 SRS4979451 GSM3893143 RNA-Seq TRANSCRIPTOMIC cDNA Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 15-90 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303893143 GSM3893143 GEO Accession GSM3893143 SRX6077643 GSM3893144 SRP190019 PRJNA530200 SRS4979452 GSM3893144 RNA-Seq TRANSCRIPTOMIC cDNA Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 15-90 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303893144 GSM3893144 GEO Accession GSM3893144 SRX6077644 GSM3893145 SRP190019 PRJNA530200 SRS4979453 GSM3893145 RNA-Seq TRANSCRIPTOMIC cDNA Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 15-90 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303893145 GSM3893145 GEO Accession GSM3893145 SRX6077645 GSM3893146 SRP190019 PRJNA530200 SRS4979454 GSM3893146 RNA-Seq TRANSCRIPTOMIC cDNA Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 15-90 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303893146 GSM3893146 GEO Accession GSM3893146 SRX6077646 GSM3893147 SRP190019 PRJNA530200 SRS4979455 GSM3893147 RNA-Seq TRANSCRIPTOMIC cDNA Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 15-90 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303893147 GSM3893147 GEO Accession GSM3893147 SRX6077647 GSM3893148 SRP190019 PRJNA530200 SRS4979456 GSM3893148 RNA-Seq TRANSCRIPTOMIC cDNA Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 15-90 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303893148 GSM3893148 GEO Accession GSM3893148 SRX6077648 GSM3893149 SRP190019 PRJNA530200 SRS4979457 GSM3893149 RNA-Seq TRANSCRIPTOMIC cDNA Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 15-90 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303893149 GSM3893149 GEO Accession GSM3893149 SRX6077649 GSM3893150 SRP190019 PRJNA530200 SRS4979458 GSM3893150 RNA-Seq TRANSCRIPTOMIC cDNA Monosomes or disomes were isolated by sucrose gradient centrifugation after RNaseI treatment. RNA was extracted using SDS/hot phenol/chloroform. Fragments ranging from 15-34 nt or 15-90 nt were gel purified for monosome or disome footprints, respectively. rRNA was depleted from this pool through Ribo-Zero Gold treatment. Upon dephosphorylation of sample RNA, linker was ligated and this product was once again gel purified. This was followed by reverse transcription as well as circularization of cDNAs. PCR amplification of this library was then sent for sequencing. Illumina HiSeq 2500 gds 303893150 GSM3893150 GEO Accession GSM3893150