SRX18367861 GSM6754319_r1 SRP409520 PRJNA904775 SRS15854293 GSM6754319 GSM6754319 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367862 GSM6754320_r1 SRP409520 PRJNA904775 SRS15854294 GSM6754320 GSM6754320 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367863 GSM6754321_r1 SRP409520 PRJNA904775 SRS15854295 GSM6754321 GSM6754321 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367864 GSM6754322_r1 SRP409520 PRJNA904775 SRS15854296 GSM6754322 GSM6754322 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367865 GSM6754323_r1 SRP409520 PRJNA904775 SRS15854297 GSM6754323 GSM6754323 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367866 GSM6754324_r1 SRP409520 PRJNA904775 SRS15854298 GSM6754324 GSM6754324 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367867 GSM6754325_r1 SRP409520 PRJNA904775 SRS15854299 GSM6754325 GSM6754325 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367868 GSM6754326_r1 SRP409520 PRJNA904775 SRS15854300 GSM6754326 GSM6754326 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367869 GSM6754327_r1 SRP409520 PRJNA904775 SRS15854301 GSM6754327 GSM6754327 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367870 GSM6754328_r1 SRP409520 PRJNA904775 SRS15854302 GSM6754328 GSM6754328 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367871 GSM6754329_r1 SRP409520 PRJNA904775 SRS15854303 GSM6754329 GSM6754329 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367872 GSM6754330_r1 SRP409520 PRJNA904775 SRS15854304 GSM6754330 GSM6754330 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367873 GSM6754331_r1 SRP409520 PRJNA904775 SRS15854305 GSM6754331 GSM6754331 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367874 GSM6754332_r1 SRP409520 PRJNA904775 SRS15854306 GSM6754332 GSM6754332 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367875 GSM6754333_r1 SRP409520 PRJNA904775 SRS15854307 GSM6754333 GSM6754333 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367876 GSM6754334_r1 SRP409520 PRJNA904775 SRS15854308 GSM6754334 GSM6754334 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367877 GSM6754335_r1 SRP409520 PRJNA904775 SRS15854309 GSM6754335 GSM6754335 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367878 GSM6754336_r1 SRP409520 PRJNA904775 SRS15854310 GSM6754336 GSM6754336 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367879 GSM6754337_r1 SRP409520 PRJNA904775 SRS15854311 GSM6754337 GSM6754337 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367880 GSM6754338_r1 SRP409520 PRJNA904775 SRS15854312 GSM6754338 GSM6754338 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367881 GSM6754339_r1 SRP409520 PRJNA904775 SRS15854313 GSM6754339 GSM6754339 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367882 GSM6754340_r1 SRP409520 PRJNA904775 SRS15854314 GSM6754340 GSM6754340 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367883 GSM6754341_r1 SRP409520 PRJNA904775 SRS15854315 GSM6754341 GSM6754341 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367884 GSM6754342_r1 SRP409520 PRJNA904775 SRS15854316 GSM6754342 GSM6754342 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367885 GSM6754343_r1 SRP409520 PRJNA904775 SRS15854317 GSM6754343 GSM6754343 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367886 GSM6754344_r1 SRP409520 PRJNA904775 SRS15854318 GSM6754344 GSM6754344 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367887 GSM6754345_r1 SRP409520 PRJNA904775 SRS15854319 GSM6754345 GSM6754345 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367888 GSM6754346_r1 SRP409520 PRJNA904775 SRS15854320 GSM6754346 GSM6754346 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367889 GSM6754347_r1 SRP409520 PRJNA904775 SRS15854321 GSM6754347 GSM6754347 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367890 GSM6754348_r1 SRP409520 PRJNA904775 SRS15854322 GSM6754348 GSM6754348 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367891 GSM6754349_r1 SRP409520 PRJNA904775 SRS15854323 GSM6754349 GSM6754349 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367892 GSM6754350_r1 SRP409520 PRJNA904775 SRS15854324 GSM6754350 GSM6754350 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367893 GSM6754351_r1 SRP409520 PRJNA904775 SRS15854325 GSM6754351 GSM6754351 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367894 GSM6754352_r1 SRP409520 PRJNA904775 SRS15854326 GSM6754352 GSM6754352 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367895 GSM6754353_r1 SRP409520 PRJNA904775 SRS15854327 GSM6754353 GSM6754353 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000 SRX18367896 GSM6754354_r1 SRP409520 PRJNA904775 SRS15854328 GSM6754354 GSM6754354 RNA-Seq TRANSCRIPTOMIC cDNA PB samples at pre-treatment, 4 - and 24 hours after start of treatment for RNA sequencing was sampled in BC Vacutainer CPTTM Mononuclear cell preparation tubes with sodium heparin. Mononuclear cells were prepared by density gradient separation (Lymphoprep, Axis-shield). For RNA sequencing, approximately 1x10^6 cells were dissolved in TRIzolTM Reagent (Thermo Fisher) and stored at -80°C until analysis. Illumina TruSeq Stranded Total RNA Illumina HiSeq 4000