SRX9687521 GSM4976172 SRP298036 SRS7885096 GSM4976172 RNA-Seq TRANSCRIPTOMIC cDNA Pellets were thawed on ice and resuspended in RNAase free water, 50 mL of 0.1 mm silica spheres (MP Lysing Matrix B) were added, and samples were bead-beaten for 90 seconds in three intervals at 4°C. Total RNA was then extracted using the MasterPure Complete RNA Purification kit (Lucigen). Genomic DNA was removed using the Turbo DNA-free kit (Ambion). Total RNA was measured with an Agilent 2100 Bioanalyzer (Agilent Technologies). The libraries were prepared using the Ribo-Zero Magnetic Kit (Bacteria; Epicentre) and the KAPA RNA HyperPrep kit (Kapa Biosystems). Library sequencing was performed using the Illumina HiSeq 2000 platform with a single-end protocol and read lengths of 40 nucleotides. Samples were stored at -20°C. Total RNA (depleted of rRNA) was converted to cDNA and sequenced with Illumina HiSeq 2000 with a single-end protocol and read lengths of 40 nucleotides Illumina HiSeq 2000 gds 304976172 GSM4976172 GEO Accession GSM4976172 SRX9687522 GSM4976173 SRP298036 SRS7885097 GSM4976173 RNA-Seq TRANSCRIPTOMIC cDNA Pellets were thawed on ice and resuspended in RNAase free water, 50 mL of 0.1 mm silica spheres (MP Lysing Matrix B) were added, and samples were bead-beaten for 90 seconds in three intervals at 4°C. Total RNA was then extracted using the MasterPure Complete RNA Purification kit (Lucigen). Genomic DNA was removed using the Turbo DNA-free kit (Ambion). Total RNA was measured with an Agilent 2100 Bioanalyzer (Agilent Technologies). The libraries were prepared using the Ribo-Zero Magnetic Kit (Bacteria; Epicentre) and the KAPA RNA HyperPrep kit (Kapa Biosystems). Library sequencing was performed using the Illumina HiSeq 2000 platform with a single-end protocol and read lengths of 40 nucleotides. Samples were stored at -20°C. Total RNA (depleted of rRNA) was converted to cDNA and sequenced with Illumina HiSeq 2000 with a single-end protocol and read lengths of 40 nucleotides Illumina HiSeq 2000 gds 304976173 GSM4976173 GEO Accession GSM4976173 SRX9687523 GSM4976174 SRP298036 SRS7885098 GSM4976174 RNA-Seq TRANSCRIPTOMIC cDNA Pellets were thawed on ice and resuspended in RNAase free water, 50 mL of 0.1 mm silica spheres (MP Lysing Matrix B) were added, and samples were bead-beaten for 90 seconds in three intervals at 4°C. Total RNA was then extracted using the MasterPure Complete RNA Purification kit (Lucigen). Genomic DNA was removed using the Turbo DNA-free kit (Ambion). Total RNA was measured with an Agilent 2100 Bioanalyzer (Agilent Technologies). The libraries were prepared using the Ribo-Zero Magnetic Kit (Bacteria; Epicentre) and the KAPA RNA HyperPrep kit (Kapa Biosystems). Library sequencing was performed using the Illumina HiSeq 2000 platform with a single-end protocol and read lengths of 40 nucleotides. Samples were stored at -20°C. Total RNA (depleted of rRNA) was converted to cDNA and sequenced with Illumina HiSeq 2000 with a single-end protocol and read lengths of 40 nucleotides Illumina HiSeq 2000 gds 304976174 GSM4976174 GEO Accession GSM4976174 SRX9687524 GSM4976175 SRP298036 SRS7885099 GSM4976175 RNA-Seq TRANSCRIPTOMIC cDNA Pellets were thawed on ice and resuspended in RNAase free water, 50 mL of 0.1 mm silica spheres (MP Lysing Matrix B) were added, and samples were bead-beaten for 90 seconds in three intervals at 4°C. Total RNA was then extracted using the MasterPure Complete RNA Purification kit (Lucigen). Genomic DNA was removed using the Turbo DNA-free kit (Ambion). Total RNA was measured with an Agilent 2100 Bioanalyzer (Agilent Technologies). The libraries were prepared using the Ribo-Zero Magnetic Kit (Bacteria; Epicentre) and the KAPA RNA HyperPrep kit (Kapa Biosystems). Library sequencing was performed using the Illumina HiSeq 2000 platform with a single-end protocol and read lengths of 40 nucleotides. Samples were stored at -20°C. Total RNA (depleted of rRNA) was converted to cDNA and sequenced with Illumina HiSeq 2000 with a single-end protocol and read lengths of 40 nucleotides Illumina HiSeq 2000 gds 304976175 GSM4976175 GEO Accession GSM4976175 SRX9687525 GSM4976176 SRP298036 SRS7885100 GSM4976176 RNA-Seq TRANSCRIPTOMIC cDNA Pellets were thawed on ice and resuspended in RNAase free water, 50 mL of 0.1 mm silica spheres (MP Lysing Matrix B) were added, and samples were bead-beaten for 90 seconds in three intervals at 4°C. Total RNA was then extracted using the MasterPure Complete RNA Purification kit (Lucigen). Genomic DNA was removed using the Turbo DNA-free kit (Ambion). Total RNA was measured with an Agilent 2100 Bioanalyzer (Agilent Technologies). The libraries were prepared using the Ribo-Zero Magnetic Kit (Bacteria; Epicentre) and the KAPA RNA HyperPrep kit (Kapa Biosystems). Library sequencing was performed using the Illumina HiSeq 2000 platform with a single-end protocol and read lengths of 40 nucleotides. Samples were stored at -20°C. Total RNA (depleted of rRNA) was converted to cDNA and sequenced with Illumina HiSeq 2000 with a single-end protocol and read lengths of 40 nucleotides Illumina HiSeq 2000 gds 304976176 GSM4976176 GEO Accession GSM4976176 SRX9687526 GSM4976177 SRP298036 SRS7885101 GSM4976177 RNA-Seq TRANSCRIPTOMIC cDNA Pellets were thawed on ice and resuspended in RNAase free water, 50 mL of 0.1 mm silica spheres (MP Lysing Matrix B) were added, and samples were bead-beaten for 90 seconds in three intervals at 4°C. Total RNA was then extracted using the MasterPure Complete RNA Purification kit (Lucigen). Genomic DNA was removed using the Turbo DNA-free kit (Ambion). Total RNA was measured with an Agilent 2100 Bioanalyzer (Agilent Technologies). The libraries were prepared using the Ribo-Zero Magnetic Kit (Bacteria; Epicentre) and the KAPA RNA HyperPrep kit (Kapa Biosystems). Library sequencing was performed using the Illumina HiSeq 2000 platform with a single-end protocol and read lengths of 40 nucleotides. Samples were stored at -20°C. Total RNA (depleted of rRNA) was converted to cDNA and sequenced with Illumina HiSeq 2000 with a single-end protocol and read lengths of 40 nucleotides Illumina HiSeq 2000 gds 304976177 GSM4976177 GEO Accession GSM4976177 SRX9687527 GSM4976178 SRP298036 SRS7885102 GSM4976178 RNA-Seq TRANSCRIPTOMIC cDNA Pellets were thawed on ice and resuspended in RNAase free water, 50 mL of 0.1 mm silica spheres (MP Lysing Matrix B) were added, and samples were bead-beaten for 90 seconds in three intervals at 4°C. Total RNA was then extracted using the MasterPure Complete RNA Purification kit (Lucigen). Genomic DNA was removed using the Turbo DNA-free kit (Ambion). Total RNA was measured with an Agilent 2100 Bioanalyzer (Agilent Technologies). The libraries were prepared using the Ribo-Zero Magnetic Kit (Bacteria; Epicentre) and the KAPA RNA HyperPrep kit (Kapa Biosystems). Library sequencing was performed using the Illumina HiSeq 2000 platform with a single-end protocol and read lengths of 40 nucleotides. Samples were stored at -20°C. Total RNA (depleted of rRNA) was converted to cDNA and sequenced with Illumina HiSeq 2000 with a single-end protocol and read lengths of 40 nucleotides Illumina HiSeq 2000 gds 304976178 GSM4976178 GEO Accession GSM4976178 SRX9687528 GSM4976179 SRP298036 SRS7885103 GSM4976179 RNA-Seq TRANSCRIPTOMIC cDNA Pellets were thawed on ice and resuspended in RNAase free water, 50 mL of 0.1 mm silica spheres (MP Lysing Matrix B) were added, and samples were bead-beaten for 90 seconds in three intervals at 4°C. Total RNA was then extracted using the MasterPure Complete RNA Purification kit (Lucigen). Genomic DNA was removed using the Turbo DNA-free kit (Ambion). Total RNA was measured with an Agilent 2100 Bioanalyzer (Agilent Technologies). The libraries were prepared using the Ribo-Zero Magnetic Kit (Bacteria; Epicentre) and the KAPA RNA HyperPrep kit (Kapa Biosystems). Library sequencing was performed using the Illumina HiSeq 2000 platform with a single-end protocol and read lengths of 40 nucleotides. Samples were stored at -20°C. Total RNA (depleted of rRNA) was converted to cDNA and sequenced with Illumina HiSeq 2000 with a single-end protocol and read lengths of 40 nucleotides Illumina HiSeq 2000 gds 304976179 GSM4976179 GEO Accession GSM4976179