SRX23783313 GSM8118295_r1 SRP492380 PRJNA1081879 SRS20607448 GSM8118295 GSM8118295 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783314 GSM8118296_r1 SRP492380 PRJNA1081879 SRS20607449 GSM8118296 GSM8118296 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783315 GSM8118377_r1 SRP492380 PRJNA1081879 SRS20607451 GSM8118377 GSM8118377 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783316 GSM8118297_r1 SRP492380 PRJNA1081879 SRS20607450 GSM8118297 GSM8118297 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783317 GSM8118298_r1 SRP492380 PRJNA1081879 SRS20607452 GSM8118298 GSM8118298 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783318 GSM8118299_r1 SRP492380 PRJNA1081879 SRS20607455 GSM8118299 GSM8118299 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783319 GSM8118300_r1 SRP492380 PRJNA1081879 SRS20607454 GSM8118300 GSM8118300 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783320 GSM8118301_r1 SRP492380 PRJNA1081879 SRS20607453 GSM8118301 GSM8118301 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783321 GSM8118302_r1 SRP492380 PRJNA1081879 SRS20607456 GSM8118302 GSM8118302 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783322 GSM8118303_r1 SRP492380 PRJNA1081879 SRS20607457 GSM8118303 GSM8118303 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783323 GSM8118304_r1 SRP492380 PRJNA1081879 SRS20607458 GSM8118304 GSM8118304 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783324 GSM8118305_r1 SRP492380 PRJNA1081879 SRS20607459 GSM8118305 GSM8118305 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783325 GSM8118306_r1 SRP492380 PRJNA1081879 SRS20607460 GSM8118306 GSM8118306 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783326 GSM8118307_r1 SRP492380 PRJNA1081879 SRS20607461 GSM8118307 GSM8118307 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783327 GSM8118308_r1 SRP492380 PRJNA1081879 SRS20607462 GSM8118308 GSM8118308 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783328 GSM8118309_r1 SRP492380 PRJNA1081879 SRS20607463 GSM8118309 GSM8118309 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783329 GSM8118310_r1 SRP492380 PRJNA1081879 SRS20607464 GSM8118310 GSM8118310 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783330 GSM8118311_r1 SRP492380 PRJNA1081879 SRS20607465 GSM8118311 GSM8118311 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783331 GSM8118312_r1 SRP492380 PRJNA1081879 SRS20607466 GSM8118312 GSM8118312 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783332 GSM8118329_r1 SRP492380 PRJNA1081879 SRS20607467 GSM8118329 GSM8118329 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783333 GSM8118330_r1 SRP492380 PRJNA1081879 SRS20607468 GSM8118330 GSM8118330 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783334 GSM8118331_r1 SRP492380 PRJNA1081879 SRS20607469 GSM8118331 GSM8118331 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783335 GSM8118332_r1 SRP492380 PRJNA1081879 SRS20607470 GSM8118332 GSM8118332 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783336 GSM8118333_r1 SRP492380 PRJNA1081879 SRS20607471 GSM8118333 GSM8118333 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783337 GSM8118334_r1 SRP492380 PRJNA1081879 SRS20607472 GSM8118334 GSM8118334 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783338 GSM8118335_r1 SRP492380 PRJNA1081879 SRS20607473 GSM8118335 GSM8118335 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783339 GSM8118336_r1 SRP492380 PRJNA1081879 SRS20607474 GSM8118336 GSM8118336 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783340 GSM8118337_r1 SRP492380 PRJNA1081879 SRS20607475 GSM8118337 GSM8118337 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783341 GSM8118338_r1 SRP492380 PRJNA1081879 SRS20607476 GSM8118338 GSM8118338 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783342 GSM8118339_r1 SRP492380 PRJNA1081879 SRS20607477 GSM8118339 GSM8118339 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783343 GSM8118340_r1 SRP492380 PRJNA1081879 SRS20607478 GSM8118340 GSM8118340 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783344 GSM8118341_r1 SRP492380 PRJNA1081879 SRS20607480 GSM8118341 GSM8118341 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783345 GSM8118342_r1 SRP492380 PRJNA1081879 SRS20607479 GSM8118342 GSM8118342 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783346 GSM8118343_r1 SRP492380 PRJNA1081879 SRS20607481 GSM8118343 GSM8118343 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783347 GSM8118344_r1 SRP492380 PRJNA1081879 SRS20607482 GSM8118344 GSM8118344 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783348 GSM8118313_r1 SRP492380 PRJNA1081879 SRS20607483 GSM8118313 GSM8118313 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783349 GSM8118314_r1 SRP492380 PRJNA1081879 SRS20607484 GSM8118314 GSM8118314 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783350 GSM8118315_r1 SRP492380 PRJNA1081879 SRS20607485 GSM8118315 GSM8118315 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783351 GSM8118316_r1 SRP492380 PRJNA1081879 SRS20607486 GSM8118316 GSM8118316 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783352 GSM8118317_r1 SRP492380 PRJNA1081879 SRS20607487 GSM8118317 GSM8118317 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783353 GSM8118318_r1 SRP492380 PRJNA1081879 SRS20607488 GSM8118318 GSM8118318 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783354 GSM8118319_r1 SRP492380 PRJNA1081879 SRS20607489 GSM8118319 GSM8118319 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783355 GSM8118320_r1 SRP492380 PRJNA1081879 SRS20607490 GSM8118320 GSM8118320 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783356 GSM8118321_r1 SRP492380 PRJNA1081879 SRS20607491 GSM8118321 GSM8118321 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783357 GSM8118322_r1 SRP492380 PRJNA1081879 SRS20607492 GSM8118322 GSM8118322 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783358 GSM8118323_r1 SRP492380 PRJNA1081879 SRS20607493 GSM8118323 GSM8118323 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783359 GSM8118324_r1 SRP492380 PRJNA1081879 SRS20607494 GSM8118324 GSM8118324 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783360 GSM8118325_r1 SRP492380 PRJNA1081879 SRS20607496 GSM8118325 GSM8118325 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783361 GSM8118326_r1 SRP492380 PRJNA1081879 SRS20607495 GSM8118326 GSM8118326 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783362 GSM8118327_r1 SRP492380 PRJNA1081879 SRS20607497 GSM8118327 GSM8118327 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783363 GSM8118328_r1 SRP492380 PRJNA1081879 SRS20607498 GSM8118328 GSM8118328 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783364 GSM8118361_r1 SRP492380 PRJNA1081879 SRS20607499 GSM8118361 GSM8118361 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783365 GSM8118362_r1 SRP492380 PRJNA1081879 SRS20607500 GSM8118362 GSM8118362 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783366 GSM8118363_r1 SRP492380 PRJNA1081879 SRS20607501 GSM8118363 GSM8118363 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783367 GSM8118364_r1 SRP492380 PRJNA1081879 SRS20607502 GSM8118364 GSM8118364 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783368 GSM8118365_r1 SRP492380 PRJNA1081879 SRS20607503 GSM8118365 GSM8118365 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783369 GSM8118366_r1 SRP492380 PRJNA1081879 SRS20607504 GSM8118366 GSM8118366 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783370 GSM8118367_r1 SRP492380 PRJNA1081879 SRS20607505 GSM8118367 GSM8118367 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783371 GSM8118368_r1 SRP492380 PRJNA1081879 SRS20607506 GSM8118368 GSM8118368 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783372 GSM8118369_r1 SRP492380 PRJNA1081879 SRS20607507 GSM8118369 GSM8118369 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783373 GSM8118370_r1 SRP492380 PRJNA1081879 SRS20607508 GSM8118370 GSM8118370 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783374 GSM8118371_r1 SRP492380 PRJNA1081879 SRS20607510 GSM8118371 GSM8118371 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783375 GSM8118372_r1 SRP492380 PRJNA1081879 SRS20607509 GSM8118372 GSM8118372 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783376 GSM8118373_r1 SRP492380 PRJNA1081879 SRS20607511 GSM8118373 GSM8118373 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783377 GSM8118374_r1 SRP492380 PRJNA1081879 SRS20607512 GSM8118374 GSM8118374 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783378 GSM8118375_r1 SRP492380 PRJNA1081879 SRS20607513 GSM8118375 GSM8118375 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783379 GSM8118376_r1 SRP492380 PRJNA1081879 SRS20607514 GSM8118376 GSM8118376 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783380 GSM8118345_r1 SRP492380 PRJNA1081879 SRS20607515 GSM8118345 GSM8118345 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783381 GSM8118346_r1 SRP492380 PRJNA1081879 SRS20607516 GSM8118346 GSM8118346 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783382 GSM8118347_r1 SRP492380 PRJNA1081879 SRS20607517 GSM8118347 GSM8118347 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783383 GSM8118348_r1 SRP492380 PRJNA1081879 SRS20607518 GSM8118348 GSM8118348 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783384 GSM8118349_r1 SRP492380 PRJNA1081879 SRS20607519 GSM8118349 GSM8118349 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783385 GSM8118350_r1 SRP492380 PRJNA1081879 SRS20607520 GSM8118350 GSM8118350 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783386 GSM8118351_r1 SRP492380 PRJNA1081879 SRS20607521 GSM8118351 GSM8118351 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783387 GSM8118352_r1 SRP492380 PRJNA1081879 SRS20607522 GSM8118352 GSM8118352 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783388 GSM8118353_r1 SRP492380 PRJNA1081879 SRS20607523 GSM8118353 GSM8118353 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783389 GSM8118354_r1 SRP492380 PRJNA1081879 SRS20607524 GSM8118354 GSM8118354 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783390 GSM8118355_r1 SRP492380 PRJNA1081879 SRS20607525 GSM8118355 GSM8118355 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783391 GSM8118356_r1 SRP492380 PRJNA1081879 SRS20607526 GSM8118356 GSM8118356 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783392 GSM8118357_r1 SRP492380 PRJNA1081879 SRS20607528 GSM8118357 GSM8118357 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783393 GSM8118358_r1 SRP492380 PRJNA1081879 SRS20607527 GSM8118358 GSM8118358 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783394 GSM8118359_r1 SRP492380 PRJNA1081879 SRS20607529 GSM8118359 GSM8118359 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000 SRX23783395 GSM8118360_r1 SRP492380 PRJNA1081879 SRS20607530 GSM8118360 GSM8118360 RNA-Seq TRANSCRIPTOMIC cDNA RNA was extracted using Trizol/BCP and Rneasy mini kit (QIAgen) and quantified using Qubit Flurometer messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand of cDNA was synthesized using random hexamer primers, followed by the second strand of cDNA synthesis. This was followed by end repair, A-tailing, adapter ligation, size selection, amplification and purification. The library was checked with Qubit and real-time PCR for quantification and bioanalyzer for size distribution detection. Illumina NovaSeq 6000