ERX6137329 E-MTAB-10867:MD038_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423598 SAMEA9699368 MD038_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound none Experimental Factor: stimulus interferon beta, 20 nanogram per milliliter ERX6137330 E-MTAB-10867:MD044_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423599 SAMEA9699369 MD044_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound none Experimental Factor: stimulus interferon beta, 20 nanogram per milliliter ERX6137331 E-MTAB-10867:MD050_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423600 SAMEA9699370 MD050_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound none Experimental Factor: stimulus interferon beta, 20 nanogram per milliliter ERX6137332 E-MTAB-10867:MD039_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423601 SAMEA9699371 MD039_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound none Experimental Factor: stimulus interferon gamma, 40 nanogram per milliliter ERX6137333 E-MTAB-10867:MD045_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423602 SAMEA9699372 MD045_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound none Experimental Factor: stimulus interferon gamma, 40 nanogram per milliliter ERX6137334 E-MTAB-10867:MD051_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423603 SAMEA9699373 MD051_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound none Experimental Factor: stimulus interferon gamma, 40 nanogram per milliliter ERX6137335 E-MTAB-10867:MD036_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423604 SAMEA9699374 MD036_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound none Experimental Factor: stimulus none ERX6137336 E-MTAB-10867:MD042_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423605 SAMEA9699375 MD042_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound none Experimental Factor: stimulus none ERX6137337 E-MTAB-10867:MD048_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423606 SAMEA9699376 MD048_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound none Experimental Factor: stimulus none ERX6137338 E-MTAB-10867:MD040_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423607 SAMEA9699377 MD040_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound arachidonic acid Experimental Factor: dose 50 Experimental Factor: stimulus interferon beta, 20 nanogram per milliliter ERX6137339 E-MTAB-10867:MD046_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423608 SAMEA9699378 MD046_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound arachidonic acid Experimental Factor: dose 50 Experimental Factor: stimulus interferon beta, 20 nanogram per milliliter ERX6137340 E-MTAB-10867:MD052_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423609 SAMEA9699379 MD052_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound arachidonic acid Experimental Factor: dose 50 Experimental Factor: stimulus interferon beta, 20 nanogram per milliliter ERX6137341 E-MTAB-10867:MD041_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423610 SAMEA9699380 MD041_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound arachidonic acid Experimental Factor: dose 50 Experimental Factor: stimulus interferon gamma, 40 nanogram per milliliter ERX6137342 E-MTAB-10867:MD047_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423611 SAMEA9699381 MD047_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound arachidonic acid Experimental Factor: dose 50 Experimental Factor: stimulus interferon gamma, 40 nanogram per milliliter ERX6137343 E-MTAB-10867:MD053_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423612 SAMEA9699382 MD053_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound arachidonic acid Experimental Factor: dose 50 Experimental Factor: stimulus interferon gamma, 40 nanogram per milliliter ERX6137344 E-MTAB-10867:MD037_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423613 SAMEA9699383 MD037_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound arachidonic acid Experimental Factor: dose 50 Experimental Factor: stimulus none ERX6137345 E-MTAB-10867:MD043_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423614 SAMEA9699384 MD043_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound arachidonic acid Experimental Factor: dose 50 Experimental Factor: stimulus none ERX6137346 E-MTAB-10867:MD049_s ERP131279 PRJEB47040 RNA-seq of monocyte derived macrophages exposed to arachidonic acid, interferon beta, or interferon gamma ERS7423615 SAMEA9699385 MD049_s RNA-Seq TRANSCRIPTOMIC PolyA cells were scrapped from culture dishes monocytes differentiated into MDMs , cultured in R5 media (RPMI + 5 % human AB Serum + 1 % Sodium Pyruvate. Media was changed 2 hours before treatment Substances were applied for 3h before harvesting. RNA was extracted using nucleospin rna extraction protocol, followed by DNA digestion using \"DNA-free™ DNA Removal Kit \" from Thermo Fisher RNA-Seq libraries were constructed 'Lexogen Quantseq 3'mRNA-seq Library Prep Kit FWD for Illumina' (Lexogen, Vienna, Austria) in combination with the 'Lexogen UMI Second Strand Synthesis Module for QuantSeq FWD (Illumina, Read 1)', NextSeq 550 Experimental Factor: compound arachidonic acid Experimental Factor: dose 50 Experimental Factor: stimulus none