SRX5626460 GSM3703281 SRP190207 SRS4572005 GSM3703281 RNA-Seq TRANSCRIPTOMIC cDNA At the end of the 4-day knockdown, Drosophila S2 cells were harvested. Human HEK293T cells were added to the harvested S2 cells (0.8x10e6 human cells / 15x10e6 S2 cells) as spike-in control. Each Pool of S2 and HEK293T cells was washed twice using 1 X PBS. Total RNA was extracted using the QIAGEN RNeasy mini kit. Libraries were prepared using the Illumina TruSeq Standard mRNA LT sample prep kit and sequenced on the Illumina HiSeq 2500 platform. RNA-seq libraries were generated from 1ug of high quality total RNA, as assessed using the Bioanalyzer (Agilent). Libraries were made according to the manufacturer's directions using the TruSeq Stranded mRNA LT Sample Prep Kit – set A (Illumina, Cat. No. RS-122-2101) kit. The resulting short fragment libraries were checked for quality and quantity using the Bioanalyzer (Agilent) and Qubit Fluorometer (Life Technologies). Libraries were pooled, re-quantified and sequenced as 50 bp single reads on the Illumina HiSeq 2500 instrument. Illumina HiSeq 2500 gds 303703281 GSM3703281 GEO Accession GSM3703281 SRX5626461 GSM3703282 SRP190207 SRS4572006 GSM3703282 RNA-Seq TRANSCRIPTOMIC cDNA At the end of the 4-day knockdown, Drosophila S2 cells were harvested. Human HEK293T cells were added to the harvested S2 cells (0.8x10e6 human cells / 15x10e6 S2 cells) as spike-in control. Each Pool of S2 and HEK293T cells was washed twice using 1 X PBS. Total RNA was extracted using the QIAGEN RNeasy mini kit. Libraries were prepared using the Illumina TruSeq Standard mRNA LT sample prep kit and sequenced on the Illumina HiSeq 2500 platform. RNA-seq libraries were generated from 1ug of high quality total RNA, as assessed using the Bioanalyzer (Agilent). Libraries were made according to the manufacturer's directions using the TruSeq Stranded mRNA LT Sample Prep Kit – set A (Illumina, Cat. No. RS-122-2101) kit. The resulting short fragment libraries were checked for quality and quantity using the Bioanalyzer (Agilent) and Qubit Fluorometer (Life Technologies). Libraries were pooled, re-quantified and sequenced as 50 bp single reads on the Illumina HiSeq 2500 instrument. Illumina HiSeq 2500 gds 303703282 GSM3703282 GEO Accession GSM3703282 SRX5626462 GSM3703283 SRP190207 SRS4572007 GSM3703283 RNA-Seq TRANSCRIPTOMIC cDNA At the end of the 4-day knockdown, Drosophila S2 cells were harvested. Human HEK293T cells were added to the harvested S2 cells (0.8x10e6 human cells / 15x10e6 S2 cells) as spike-in control. Each Pool of S2 and HEK293T cells was washed twice using 1 X PBS. Total RNA was extracted using the QIAGEN RNeasy mini kit. Libraries were prepared using the Illumina TruSeq Standard mRNA LT sample prep kit and sequenced on the Illumina HiSeq 2500 platform. RNA-seq libraries were generated from 1ug of high quality total RNA, as assessed using the Bioanalyzer (Agilent). Libraries were made according to the manufacturer's directions using the TruSeq Stranded mRNA LT Sample Prep Kit – set A (Illumina, Cat. No. RS-122-2101) kit. The resulting short fragment libraries were checked for quality and quantity using the Bioanalyzer (Agilent) and Qubit Fluorometer (Life Technologies). Libraries were pooled, re-quantified and sequenced as 50 bp single reads on the Illumina HiSeq 2500 instrument. Illumina HiSeq 2500 gds 303703283 GSM3703283 GEO Accession GSM3703283 SRX5626463 GSM3703284 SRP190207 SRS4572008 GSM3703284 RNA-Seq TRANSCRIPTOMIC cDNA At the end of the 4-day knockdown, Drosophila S2 cells were harvested. Human HEK293T cells were added to the harvested S2 cells (0.8x10e6 human cells / 15x10e6 S2 cells) as spike-in control. Each Pool of S2 and HEK293T cells was washed twice using 1 X PBS. Total RNA was extracted using the QIAGEN RNeasy mini kit. Libraries were prepared using the Illumina TruSeq Standard mRNA LT sample prep kit and sequenced on the Illumina HiSeq 2500 platform. RNA-seq libraries were generated from 1ug of high quality total RNA, as assessed using the Bioanalyzer (Agilent). Libraries were made according to the manufacturer's directions using the TruSeq Stranded mRNA LT Sample Prep Kit – set A (Illumina, Cat. No. RS-122-2101) kit. The resulting short fragment libraries were checked for quality and quantity using the Bioanalyzer (Agilent) and Qubit Fluorometer (Life Technologies). Libraries were pooled, re-quantified and sequenced as 50 bp single reads on the Illumina HiSeq 2500 instrument. Illumina HiSeq 2500 gds 303703284 GSM3703284 GEO Accession GSM3703284 SRX5626464 GSM3703285 SRP190207 SRS4572009 GSM3703285 RNA-Seq TRANSCRIPTOMIC cDNA At the end of the 4-day knockdown, Drosophila S2 cells were harvested. Human HEK293T cells were added to the harvested S2 cells (0.8x10e6 human cells / 15x10e6 S2 cells) as spike-in control. Each Pool of S2 and HEK293T cells was washed twice using 1 X PBS. Total RNA was extracted using the QIAGEN RNeasy mini kit. Libraries were prepared using the Illumina TruSeq Standard mRNA LT sample prep kit and sequenced on the Illumina HiSeq 2500 platform. RNA-seq libraries were generated from 1ug of high quality total RNA, as assessed using the Bioanalyzer (Agilent). Libraries were made according to the manufacturer's directions using the TruSeq Stranded mRNA LT Sample Prep Kit – set A (Illumina, Cat. No. RS-122-2101) kit. The resulting short fragment libraries were checked for quality and quantity using the Bioanalyzer (Agilent) and Qubit Fluorometer (Life Technologies). Libraries were pooled, re-quantified and sequenced as 50 bp single reads on the Illumina HiSeq 2500 instrument. Illumina HiSeq 2500 gds 303703285 GSM3703285 GEO Accession GSM3703285 SRX5626465 GSM3703286 SRP190207 SRS4572010 GSM3703286 RNA-Seq TRANSCRIPTOMIC cDNA At the end of the 4-day knockdown, Drosophila S2 cells were harvested. Human HEK293T cells were added to the harvested S2 cells (0.8x10e6 human cells / 15x10e6 S2 cells) as spike-in control. Each Pool of S2 and HEK293T cells was washed twice using 1 X PBS. Total RNA was extracted using the QIAGEN RNeasy mini kit. Libraries were prepared using the Illumina TruSeq Standard mRNA LT sample prep kit and sequenced on the Illumina HiSeq 2500 platform. RNA-seq libraries were generated from 1ug of high quality total RNA, as assessed using the Bioanalyzer (Agilent). Libraries were made according to the manufacturer's directions using the TruSeq Stranded mRNA LT Sample Prep Kit – set A (Illumina, Cat. No. RS-122-2101) kit. The resulting short fragment libraries were checked for quality and quantity using the Bioanalyzer (Agilent) and Qubit Fluorometer (Life Technologies). Libraries were pooled, re-quantified and sequenced as 50 bp single reads on the Illumina HiSeq 2500 instrument. Illumina HiSeq 2500 gds 303703286 GSM3703286 GEO Accession GSM3703286 SRX5626466 GSM3703287 SRP190207 SRS4572012 GSM3703287 RNA-Seq TRANSCRIPTOMIC cDNA At the end of the 4-day knockdown, Drosophila S2 cells were harvested. Human HEK293T cells were added to the harvested S2 cells (0.8x10e6 human cells / 15x10e6 S2 cells) as spike-in control. Each Pool of S2 and HEK293T cells was washed twice using 1 X PBS. Total RNA was extracted using the QIAGEN RNeasy mini kit. Libraries were prepared using the Illumina TruSeq Standard mRNA LT sample prep kit and sequenced on the Illumina HiSeq 2500 platform. RNA-seq libraries were generated from 1ug of high quality total RNA, as assessed using the Bioanalyzer (Agilent). Libraries were made according to the manufacturer's directions using the TruSeq Stranded mRNA LT Sample Prep Kit – set A (Illumina, Cat. No. RS-122-2101) kit. The resulting short fragment libraries were checked for quality and quantity using the Bioanalyzer (Agilent) and Qubit Fluorometer (Life Technologies). Libraries were pooled, re-quantified and sequenced as 50 bp single reads on the Illumina HiSeq 2500 instrument. Illumina HiSeq 2500 gds 303703287 GSM3703287 GEO Accession GSM3703287 SRX5626467 GSM3703288 SRP190207 SRS4572013 GSM3703288 RNA-Seq TRANSCRIPTOMIC cDNA At the end of the 4-day knockdown, Drosophila S2 cells were harvested. Human HEK293T cells were added to the harvested S2 cells (0.8x10e6 human cells / 15x10e6 S2 cells) as spike-in control. Each Pool of S2 and HEK293T cells was washed twice using 1 X PBS. Total RNA was extracted using the QIAGEN RNeasy mini kit. Libraries were prepared using the Illumina TruSeq Standard mRNA LT sample prep kit and sequenced on the Illumina HiSeq 2500 platform. RNA-seq libraries were generated from 1ug of high quality total RNA, as assessed using the Bioanalyzer (Agilent). Libraries were made according to the manufacturer's directions using the TruSeq Stranded mRNA LT Sample Prep Kit – set A (Illumina, Cat. No. RS-122-2101) kit. The resulting short fragment libraries were checked for quality and quantity using the Bioanalyzer (Agilent) and Qubit Fluorometer (Life Technologies). Libraries were pooled, re-quantified and sequenced as 50 bp single reads on the Illumina HiSeq 2500 instrument. Illumina HiSeq 2500 gds 303703288 GSM3703288 GEO Accession GSM3703288 SRX5626468 GSM3703289 SRP190207 SRS4572011 GSM3703289 RNA-Seq TRANSCRIPTOMIC cDNA At the end of the 4-day knockdown, Drosophila S2 cells were harvested. Human HEK293T cells were added to the harvested S2 cells (0.8x10e6 human cells / 15x10e6 S2 cells) as spike-in control. Each Pool of S2 and HEK293T cells was washed twice using 1 X PBS. Total RNA was extracted using the QIAGEN RNeasy mini kit. Libraries were prepared using the Illumina TruSeq Standard mRNA LT sample prep kit and sequenced on the Illumina HiSeq 2500 platform. RNA-seq libraries were generated from 1ug of high quality total RNA, as assessed using the Bioanalyzer (Agilent). Libraries were made according to the manufacturer's directions using the TruSeq Stranded mRNA LT Sample Prep Kit – set A (Illumina, Cat. No. RS-122-2101) kit. The resulting short fragment libraries were checked for quality and quantity using the Bioanalyzer (Agilent) and Qubit Fluorometer (Life Technologies). Libraries were pooled, re-quantified and sequenced as 50 bp single reads on the Illumina HiSeq 2500 instrument. Illumina HiSeq 2500 gds 303703289 GSM3703289 GEO Accession GSM3703289 SRX5626469 GSM3703290 SRP190207 SRS4572014 GSM3703290 RNA-Seq TRANSCRIPTOMIC cDNA At the end of the 4-day knockdown, Drosophila S2 cells were harvested. Human HEK293T cells were added to the harvested S2 cells (0.8x10e6 human cells / 15x10e6 S2 cells) as spike-in control. Each Pool of S2 and HEK293T cells was washed twice using 1 X PBS. Total RNA was extracted using the QIAGEN RNeasy mini kit. Libraries were prepared using the Illumina TruSeq Standard mRNA LT sample prep kit and sequenced on the Illumina HiSeq 2500 platform. RNA-seq libraries were generated from 1ug of high quality total RNA, as assessed using the Bioanalyzer (Agilent). Libraries were made according to the manufacturer's directions using the TruSeq Stranded mRNA LT Sample Prep Kit – set A (Illumina, Cat. No. RS-122-2101) kit. The resulting short fragment libraries were checked for quality and quantity using the Bioanalyzer (Agilent) and Qubit Fluorometer (Life Technologies). Libraries were pooled, re-quantified and sequenced as 50 bp single reads on the Illumina HiSeq 2500 instrument. Illumina HiSeq 2500 gds 303703290 GSM3703290 GEO Accession GSM3703290