SRX3197484 GSM2787575 SRP118092 SRS2524563 GSM2787575 OTHER GENOMIC other Plasmid DNA was extracted from MegaX DH10B electrocompetent bacteria transformed with cloned library using Qiagen's Plasmid Plus MegaPrep Kit following manufacturer's instructions We used a custom library construction protocol, see Methods section in paper for detailed protocol. Briefly, for RNA, following PolyA+ selection we performed reverse transcription using a sgGFP reporter gene-specific primer and performed PCR to add barcoded Illumina sequencing adapters. For plasmid reporter library, we directly performed PCR to add sequencing adapters off of the plasmid. NextSeq 500 gds 302787575 GSM2787575 GEO Accession GSM2787575 SRX3197485 GSM2787576 SRP118092 SRS2524564 GSM2787576 OTHER GENOMIC other Plasmid DNA was extracted from MegaX DH10B electrocompetent bacteria transformed with cloned library using Qiagen's Plasmid Plus MegaPrep Kit following manufacturer's instructions We used a custom library construction protocol, see Methods section in paper for detailed protocol. Briefly, for RNA, following PolyA+ selection we performed reverse transcription using a sgGFP reporter gene-specific primer and performed PCR to add barcoded Illumina sequencing adapters. For plasmid reporter library, we directly performed PCR to add sequencing adapters off of the plasmid. NextSeq 500 gds 302787576 GSM2787576 GEO Accession GSM2787576 SRX3197486 GSM2787577 SRP118092 SRS2524565 GSM2787577 OTHER GENOMIC other Plasmid DNA was extracted from MegaX DH10B electrocompetent bacteria transformed with cloned library using Qiagen's Plasmid Plus MegaPrep Kit following manufacturer's instructions We used a custom library construction protocol, see Methods section in paper for detailed protocol. Briefly, for RNA, following PolyA+ selection we performed reverse transcription using a sgGFP reporter gene-specific primer and performed PCR to add barcoded Illumina sequencing adapters. For plasmid reporter library, we directly performed PCR to add sequencing adapters off of the plasmid. NextSeq 500 gds 302787577 GSM2787577 GEO Accession GSM2787577 SRX3197487 GSM2787578 SRP118092 SRS2524567 GSM2787578 OTHER GENOMIC other Plasmid DNA was extracted from MegaX DH10B electrocompetent bacteria transformed with cloned library using Qiagen's Plasmid Plus MegaPrep Kit following manufacturer's instructions We used a custom library construction protocol, see Methods section in paper for detailed protocol. Briefly, for RNA, following PolyA+ selection we performed reverse transcription using a sgGFP reporter gene-specific primer and performed PCR to add barcoded Illumina sequencing adapters. For plasmid reporter library, we directly performed PCR to add sequencing adapters off of the plasmid. NextSeq 500 gds 302787578 GSM2787578 GEO Accession GSM2787578 SRX3197488 GSM2787579 SRP118092 SRS2524566 GSM2787579 OTHER GENOMIC other Plasmid DNA was extracted from MegaX DH10B electrocompetent bacteria transformed with cloned library using Qiagen's Plasmid Plus MegaPrep Kit following manufacturer's instructions We used a custom library construction protocol, see Methods section in paper for detailed protocol. Briefly, for RNA, following PolyA+ selection we performed reverse transcription using a sgGFP reporter gene-specific primer and performed PCR to add barcoded Illumina sequencing adapters. For plasmid reporter library, we directly performed PCR to add sequencing adapters off of the plasmid. NextSeq 500 gds 302787579 GSM2787579 GEO Accession GSM2787579 SRX3197489 GSM2787580 SRP118092 SRS2524568 GSM2787580 RNA-Seq TRANSCRIPTOMIC cDNA RNA was collected using the Qiagen RNEasy Maxi kit following manufacturer's instructions and performing the optional on-column Dnase treatment. PolyA+ RNA was extracted using the Oligotex mRNA Midi kit. We used a custom library construction protocol, see Methods section in paper for detailed protocol. Briefly, for RNA, following PolyA+ selection we performed reverse transcription using a sgGFP reporter gene-specific primer and performed PCR to add barcoded Illumina sequencing adapters. For plasmid reporter library, we directly performed PCR to add sequencing adapters off of the plasmid. NextSeq 500 gds 302787580 GSM2787580 GEO Accession GSM2787580 SRX3197490 GSM2787581 SRP118092 SRS2524569 GSM2787581 RNA-Seq TRANSCRIPTOMIC cDNA RNA was collected using the Qiagen RNEasy Maxi kit following manufacturer's instructions and performing the optional on-column Dnase treatment. PolyA+ RNA was extracted using the Oligotex mRNA Midi kit. We used a custom library construction protocol, see Methods section in paper for detailed protocol. Briefly, for RNA, following PolyA+ selection we performed reverse transcription using a sgGFP reporter gene-specific primer and performed PCR to add barcoded Illumina sequencing adapters. For plasmid reporter library, we directly performed PCR to add sequencing adapters off of the plasmid. NextSeq 500 gds 302787581 GSM2787581 GEO Accession GSM2787581 SRX3197491 GSM2787582 SRP118092 SRS2524571 GSM2787582 RNA-Seq TRANSCRIPTOMIC cDNA RNA was collected using the Qiagen RNEasy Maxi kit following manufacturer's instructions and performing the optional on-column Dnase treatment. PolyA+ RNA was extracted using the Oligotex mRNA Midi kit. We used a custom library construction protocol, see Methods section in paper for detailed protocol. Briefly, for RNA, following PolyA+ selection we performed reverse transcription using a sgGFP reporter gene-specific primer and performed PCR to add barcoded Illumina sequencing adapters. For plasmid reporter library, we directly performed PCR to add sequencing adapters off of the plasmid. NextSeq 500 gds 302787582 GSM2787582 GEO Accession GSM2787582 SRX3197492 GSM2787583 SRP118092 SRS2524570 GSM2787583 RNA-Seq TRANSCRIPTOMIC cDNA RNA was collected using the Qiagen RNEasy Maxi kit following manufacturer's instructions and performing the optional on-column Dnase treatment. PolyA+ RNA was extracted using the Oligotex mRNA Midi kit. We used a custom library construction protocol, see Methods section in paper for detailed protocol. Briefly, for RNA, following PolyA+ selection we performed reverse transcription using a sgGFP reporter gene-specific primer and performed PCR to add barcoded Illumina sequencing adapters. For plasmid reporter library, we directly performed PCR to add sequencing adapters off of the plasmid. NextSeq 500 gds 302787583 GSM2787583 GEO Accession GSM2787583 SRX3197493 GSM2787584 SRP118092 SRS2524572 GSM2787584 RNA-Seq TRANSCRIPTOMIC cDNA RNA was collected using the Qiagen RNEasy Maxi kit following manufacturer's instructions and performing the optional on-column Dnase treatment. PolyA+ RNA was extracted using the Oligotex mRNA Midi kit. We used a custom library construction protocol, see Methods section in paper for detailed protocol. Briefly, for RNA, following PolyA+ selection we performed reverse transcription using a sgGFP reporter gene-specific primer and performed PCR to add barcoded Illumina sequencing adapters. For plasmid reporter library, we directly performed PCR to add sequencing adapters off of the plasmid. NextSeq 500 gds 302787584 GSM2787584 GEO Accession GSM2787584 SRX3197494 GSM2787585 SRP118092 SRS2524573 GSM2787585 OTHER GENOMIC other Plasmid DNA was extracted from MegaX DH10B electrocompetent bacteria transformed with cloned library using Qiagen's Plasmid Plus MegaPrep Kit following manufacturer's instructions We used a custom library construction protocol, see Methods section in paper for detailed protocol. Briefly, for RNA, following PolyA+ selection we performed reverse transcription using a sgGFP reporter gene-specific primer and performed PCR to add barcoded Illumina sequencing adapters. For plasmid reporter library, we directly performed PCR to add sequencing adapters off of the plasmid. Illumina MiSeq gds 302787585 GSM2787585 GEO Accession GSM2787585