SRX4619047 GSM3359731 GSM3359731: M. tuberculosis exposed to quinazoline-11626252 at 10x MIC, replicate 1; Mycobacterium tuberculosis; RNA-Seq SRP159028 SRS3721833 GSM3359731 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested by centrifugation and pellets were stored with 1 ml of TRIzol reagent (Thermo Fisher Scientific) at -80oC until further processed. Cells were lysed by bead-beating and total RNA was extracted by phenol-chloroform with DNAse treatment (RQ1 RNase–free DNase, Promega). Library preparation was done using the Ribo-zero rRNA removal kit (Illumina) for Gram-positive bacteria. Illumina HiSeq 2500 gds 303359731 GEO Accession GSM3359731 SRX4619048 GSM3359732 GSM3359732: M. tuberculosis exposed to quinazoline-11626252 at 10x MIC, replicate 2; Mycobacterium tuberculosis; RNA-Seq SRP159028 SRS3721834 GSM3359732 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested by centrifugation and pellets were stored with 1 ml of TRIzol reagent (Thermo Fisher Scientific) at -80oC until further processed. Cells were lysed by bead-beating and total RNA was extracted by phenol-chloroform with DNAse treatment (RQ1 RNase–free DNase, Promega). Library preparation was done using the Ribo-zero rRNA removal kit (Illumina) for Gram-positive bacteria. Illumina HiSeq 2500 gds 303359732 GEO Accession GSM3359732 SRX4619049 GSM3359733 GSM3359733: M. tuberculosis exposed to quinazoline-11626252 at 30x MIC, replicate 1; Mycobacterium tuberculosis; RNA-Seq SRP159028 SRS3721835 GSM3359733 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested by centrifugation and pellets were stored with 1 ml of TRIzol reagent (Thermo Fisher Scientific) at -80oC until further processed. Cells were lysed by bead-beating and total RNA was extracted by phenol-chloroform with DNAse treatment (RQ1 RNase–free DNase, Promega). Library preparation was done using the Ribo-zero rRNA removal kit (Illumina) for Gram-positive bacteria. Illumina HiSeq 2500 gds 303359733 GEO Accession GSM3359733 SRX4619050 GSM3359734 GSM3359734: M. tuberculosis exposed to quinazoline-11626252 at 30x MIC, replicate 2; Mycobacterium tuberculosis; RNA-Seq SRP159028 SRS3721836 GSM3359734 RNA-Seq TRANSCRIPTOMIC cDNA Cells were harvested by centrifugation and pellets were stored with 1 ml of TRIzol reagent (Thermo Fisher Scientific) at -80oC until further processed. Cells were lysed by bead-beating and total RNA was extracted by phenol-chloroform with DNAse treatment (RQ1 RNase–free DNase, Promega). Library preparation was done using the Ribo-zero rRNA removal kit (Illumina) for Gram-positive bacteria. Illumina HiSeq 2500 gds 303359734 GEO Accession GSM3359734