SRX18550889 GSM6807251_r1 SRP412201 PRJNA910517 SRS16017198 GSM6807251 GSM6807251 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550890 GSM6807252_r1 SRP412201 PRJNA910517 SRS16017197 GSM6807252 GSM6807252 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550891 GSM6807253_r1 SRP412201 PRJNA910517 SRS16017199 GSM6807253 GSM6807253 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550892 GSM6807254_r1 SRP412201 PRJNA910517 SRS16017200 GSM6807254 GSM6807254 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550893 GSM6807255_r1 SRP412201 PRJNA910517 SRS16017201 GSM6807255 GSM6807255 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550894 GSM6807256_r1 SRP412201 PRJNA910517 SRS16017202 GSM6807256 GSM6807256 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550895 GSM6807257_r1 SRP412201 PRJNA910517 SRS16017203 GSM6807257 GSM6807257 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550896 GSM6807258_r1 SRP412201 PRJNA910517 SRS16017204 GSM6807258 GSM6807258 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550897 GSM6807259_r1 SRP412201 PRJNA910517 SRS16017205 GSM6807259 GSM6807259 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550898 GSM6807260_r1 SRP412201 PRJNA910517 SRS16017206 GSM6807260 GSM6807260 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550899 GSM6807261_r1 SRP412201 PRJNA910517 SRS16017207 GSM6807261 GSM6807261 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550900 GSM6807262_r1 SRP412201 PRJNA910517 SRS16017208 GSM6807262 GSM6807262 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550904 GSM6807266_r1 SRP412201 PRJNA910517 SRS16017212 GSM6807266 GSM6807266 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550905 GSM6807267_r1 SRP412201 PRJNA910517 SRS16017213 GSM6807267 GSM6807267 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550906 GSM6807268_r1 SRP412201 PRJNA910517 SRS16017214 GSM6807268 GSM6807268 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550907 GSM6807269_r1 SRP412201 PRJNA910517 SRS16017215 GSM6807269 GSM6807269 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550908 GSM6807270_r1 SRP412201 PRJNA910517 SRS16017216 GSM6807270 GSM6807270 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550909 GSM6807271_r1 SRP412201 PRJNA910517 SRS16017217 GSM6807271 GSM6807271 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550910 GSM6807272_r1 SRP412201 PRJNA910517 SRS16017218 GSM6807272 GSM6807272 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550911 GSM6807273_r1 SRP412201 PRJNA910517 SRS16017219 GSM6807273 GSM6807273 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550912 GSM6807274_r1 SRP412201 PRJNA910517 SRS16017220 GSM6807274 GSM6807274 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550913 GSM6807275_r1 SRP412201 PRJNA910517 SRS16017221 GSM6807275 GSM6807275 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550914 GSM6807276_r1 SRP412201 PRJNA910517 SRS16017222 GSM6807276 GSM6807276 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550915 GSM6807277_r1 SRP412201 PRJNA910517 SRS16017223 GSM6807277 GSM6807277 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550916 GSM6807278_r1 SRP412201 PRJNA910517 SRS16017224 GSM6807278 GSM6807278 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550917 GSM6807279_r1 SRP412201 PRJNA910517 SRS16017225 GSM6807279 GSM6807279 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550918 GSM6807280_r1 SRP412201 PRJNA910517 SRS16017226 GSM6807280 GSM6807280 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550919 GSM6807281_r1 SRP412201 PRJNA910517 SRS16017227 GSM6807281 GSM6807281 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550920 GSM6807282_r1 SRP412201 PRJNA910517 SRS16017228 GSM6807282 GSM6807282 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550921 GSM6807283_r1 SRP412201 PRJNA910517 SRS16017229 GSM6807283 GSM6807283 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550922 GSM6807284_r1 SRP412201 PRJNA910517 SRS16017230 GSM6807284 GSM6807284 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550923 GSM6807285_r1 SRP412201 PRJNA910517 SRS16017231 GSM6807285 GSM6807285 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000 SRX18550924 GSM6807286_r1 SRP412201 PRJNA910517 SRS16017232 GSM6807286 GSM6807286 RNA-Seq TRANSCRIPTOMIC cDNA Cell pellets of approximately 500K cells were prepared in triplicate and flash frozen at the time of the experiment. RNA was extracted using the Qiagen RNeasy Plus mini kit with a genomic DNA elimination column (74104). Extracted RNA samples were submitted to Novogene for library preparation and sequencing. Briefly, RNA quality was confirmed, 150bp paired-end mRNA libraries were prepared, and libraries were sequenced at a depth of 20M reads per sample on the NovaSeq 6000 platform (Illumina). Illumina NovaSeq 6000