SRX5620810 GSM3701248 SRP190039 SRS4566980 GSM3701248 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from treated S2 cells using the EZ1 RNA Universal Kit (Quiagen). Cells were disrupted and homogenized in 750 μl QIAzol lysis reagent via bead-milling on the TissueLyser II (Qiagen). RNA was collected from the homogenate by chloroform exraction and purified on the EZ1 Advanced (Qiagen) with additional step to remove any residual DNA. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303701248 GSM3701248 GEO Accession GSM3701248 SRX5620811 GSM3701249 SRP190039 SRS4566978 GSM3701249 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from treated S2 cells using the EZ1 RNA Universal Kit (Quiagen). Cells were disrupted and homogenized in 750 μl QIAzol lysis reagent via bead-milling on the TissueLyser II (Qiagen). RNA was collected from the homogenate by chloroform exraction and purified on the EZ1 Advanced (Qiagen) with additional step to remove any residual DNA. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303701249 GSM3701249 GEO Accession GSM3701249 SRX5620812 GSM3701250 SRP190039 SRS4566979 GSM3701250 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from treated S2 cells using the EZ1 RNA Universal Kit (Quiagen). Cells were disrupted and homogenized in 750 μl QIAzol lysis reagent via bead-milling on the TissueLyser II (Qiagen). RNA was collected from the homogenate by chloroform exraction and purified on the EZ1 Advanced (Qiagen) with additional step to remove any residual DNA. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303701250 GSM3701250 GEO Accession GSM3701250 SRX5620813 GSM3701251 SRP190039 SRS4566981 GSM3701251 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from treated S2 cells using the EZ1 RNA Universal Kit (Quiagen). Cells were disrupted and homogenized in 750 μl QIAzol lysis reagent via bead-milling on the TissueLyser II (Qiagen). RNA was collected from the homogenate by chloroform exraction and purified on the EZ1 Advanced (Qiagen) with additional step to remove any residual DNA. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303701251 GSM3701251 GEO Accession GSM3701251 SRX5620814 GSM3701252 SRP190039 SRS4566982 GSM3701252 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from treated S2 cells using the EZ1 RNA Universal Kit (Quiagen). Cells were disrupted and homogenized in 750 μl QIAzol lysis reagent via bead-milling on the TissueLyser II (Qiagen). RNA was collected from the homogenate by chloroform exraction and purified on the EZ1 Advanced (Qiagen) with additional step to remove any residual DNA. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303701252 GSM3701252 GEO Accession GSM3701252 SRX5620815 GSM3701253 SRP190039 SRS4566983 GSM3701253 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from treated S2 cells using the EZ1 RNA Universal Kit (Quiagen). Cells were disrupted and homogenized in 750 μl QIAzol lysis reagent via bead-milling on the TissueLyser II (Qiagen). RNA was collected from the homogenate by chloroform exraction and purified on the EZ1 Advanced (Qiagen) with additional step to remove any residual DNA. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303701253 GSM3701253 GEO Accession GSM3701253 SRX5620816 GSM3701254 SRP190039 SRS4566984 GSM3701254 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from treated S2 cells using the EZ1 RNA Universal Kit (Quiagen). Cells were disrupted and homogenized in 750 μl QIAzol lysis reagent via bead-milling on the TissueLyser II (Qiagen). RNA was collected from the homogenate by chloroform exraction and purified on the EZ1 Advanced (Qiagen) with additional step to remove any residual DNA. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303701254 GSM3701254 GEO Accession GSM3701254 SRX5620817 GSM3701255 SRP190039 SRS4566985 GSM3701255 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from treated S2 cells using the EZ1 RNA Universal Kit (Quiagen). Cells were disrupted and homogenized in 750 μl QIAzol lysis reagent via bead-milling on the TissueLyser II (Qiagen). RNA was collected from the homogenate by chloroform exraction and purified on the EZ1 Advanced (Qiagen) with additional step to remove any residual DNA. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303701255 GSM3701255 GEO Accession GSM3701255 SRX5620818 GSM3701256 SRP190039 SRS4566986 GSM3701256 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from treated S2 cells using the EZ1 RNA Universal Kit (Quiagen). Cells were disrupted and homogenized in 750 μl QIAzol lysis reagent via bead-milling on the TissueLyser II (Qiagen). RNA was collected from the homogenate by chloroform exraction and purified on the EZ1 Advanced (Qiagen) with additional step to remove any residual DNA. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303701256 GSM3701256 GEO Accession GSM3701256 SRX5620819 GSM3701257 SRP190039 SRS4566987 GSM3701257 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from treated S2 cells using the EZ1 RNA Universal Kit (Quiagen). Cells were disrupted and homogenized in 750 μl QIAzol lysis reagent via bead-milling on the TissueLyser II (Qiagen). RNA was collected from the homogenate by chloroform exraction and purified on the EZ1 Advanced (Qiagen) with additional step to remove any residual DNA. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303701257 GSM3701257 GEO Accession GSM3701257 SRX5620820 GSM3701258 SRP190039 SRS4566988 GSM3701258 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from treated S2 cells using the EZ1 RNA Universal Kit (Quiagen). Cells were disrupted and homogenized in 750 μl QIAzol lysis reagent via bead-milling on the TissueLyser II (Qiagen). RNA was collected from the homogenate by chloroform exraction and purified on the EZ1 Advanced (Qiagen) with additional step to remove any residual DNA. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303701258 GSM3701258 GEO Accession GSM3701258 SRX5620821 GSM3701259 SRP190039 SRS4566989 GSM3701259 RNA-Seq TRANSCRIPTOMIC cDNA Total RNA was isolated from treated S2 cells using the EZ1 RNA Universal Kit (Quiagen). Cells were disrupted and homogenized in 750 μl QIAzol lysis reagent via bead-milling on the TissueLyser II (Qiagen). RNA was collected from the homogenate by chloroform exraction and purified on the EZ1 Advanced (Qiagen) with additional step to remove any residual DNA. RNA libraries were prepared for sequencing using standard Illumina protocols Illumina HiSeq 2500 gds 303701259 GSM3701259 GEO Accession GSM3701259