SRX20314414 GSM7330617_r1 SRP437492 PRJNA971941 SRS17638823 GSM7330617 GSM7330617 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314415 GSM7330618_r1 SRP437492 PRJNA971941 SRS17638824 GSM7330618 GSM7330618 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314416 GSM7330619_r1 SRP437492 PRJNA971941 SRS17638825 GSM7330619 GSM7330619 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314417 GSM7330620_r1 SRP437492 PRJNA971941 SRS17638826 GSM7330620 GSM7330620 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314418 GSM7330621_r1 SRP437492 PRJNA971941 SRS17638827 GSM7330621 GSM7330621 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314419 GSM7330622_r1 SRP437492 PRJNA971941 SRS17638828 GSM7330622 GSM7330622 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314420 GSM7330623_r1 SRP437492 PRJNA971941 SRS17638829 GSM7330623 GSM7330623 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314421 GSM7330625_r1 SRP437492 PRJNA971941 SRS17638830 GSM7330625 GSM7330625 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314422 GSM7330626_r1 SRP437492 PRJNA971941 SRS17638831 GSM7330626 GSM7330626 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314423 GSM7330627_r1 SRP437492 PRJNA971941 SRS17638832 GSM7330627 GSM7330627 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314424 GSM7330628_r1 SRP437492 PRJNA971941 SRS17638833 GSM7330628 GSM7330628 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314425 GSM7330629_r1 SRP437492 PRJNA971941 SRS17638834 GSM7330629 GSM7330629 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314426 GSM7330630_r1 SRP437492 PRJNA971941 SRS17638835 GSM7330630 GSM7330630 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314427 GSM7330631_r1 SRP437492 PRJNA971941 SRS17638836 GSM7330631 GSM7330631 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314428 GSM7330633_r1 SRP437492 PRJNA971941 SRS17638837 GSM7330633 GSM7330633 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314429 GSM7330634_r1 SRP437492 PRJNA971941 SRS17638838 GSM7330634 GSM7330634 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314430 GSM7330635_r1 SRP437492 PRJNA971941 SRS17638839 GSM7330635 GSM7330635 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314431 GSM7330636_r1 SRP437492 PRJNA971941 SRS17638840 GSM7330636 GSM7330636 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314432 GSM7330637_r1 SRP437492 PRJNA971941 SRS17638841 GSM7330637 GSM7330637 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314433 GSM7330638_r1 SRP437492 PRJNA971941 SRS17638842 GSM7330638 GSM7330638 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314435 GSM7330641_r1 SRP437492 PRJNA971941 SRS17638844 GSM7330641 GSM7330641 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314436 GSM7330642_r1 SRP437492 PRJNA971941 SRS17638845 GSM7330642 GSM7330642 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314437 GSM7330643_r1 SRP437492 PRJNA971941 SRS17638846 GSM7330643 GSM7330643 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314438 GSM7330644_r1 SRP437492 PRJNA971941 SRS17638847 GSM7330644 GSM7330644 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314439 GSM7330645_r1 SRP437492 PRJNA971941 SRS17638848 GSM7330645 GSM7330645 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314440 GSM7330647_r1 SRP437492 PRJNA971941 SRS17638849 GSM7330647 GSM7330647 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314441 GSM7330648_r1 SRP437492 PRJNA971941 SRS17638850 GSM7330648 GSM7330648 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314442 GSM7330649_r1 SRP437492 PRJNA971941 SRS17638852 GSM7330649 GSM7330649 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314443 GSM7330650_r1 SRP437492 PRJNA971941 SRS17638851 GSM7330650 GSM7330650 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314444 GSM7330652_r1 SRP437492 PRJNA971941 SRS17638853 GSM7330652 GSM7330652 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314445 GSM7330653_r1 SRP437492 PRJNA971941 SRS17638854 GSM7330653 GSM7330653 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314446 GSM7330654_r1 SRP437492 PRJNA971941 SRS17638856 GSM7330654 GSM7330654 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314447 GSM7330655_r1 SRP437492 PRJNA971941 SRS17638855 GSM7330655 GSM7330655 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314448 GSM7330656_r1 SRP437492 PRJNA971941 SRS17638857 GSM7330656 GSM7330656 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314449 GSM7330657_r1 SRP437492 PRJNA971941 SRS17638858 GSM7330657 GSM7330657 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314450 GSM7330659_r1 SRP437492 PRJNA971941 SRS17638859 GSM7330659 GSM7330659 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314451 GSM7330660_r1 SRP437492 PRJNA971941 SRS17638861 GSM7330660 GSM7330660 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314452 GSM7330661_r1 SRP437492 PRJNA971941 SRS17638860 GSM7330661 GSM7330661 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314453 GSM7330662_r1 SRP437492 PRJNA971941 SRS17638862 GSM7330662 GSM7330662 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314454 GSM7330663_r1 SRP437492 PRJNA971941 SRS17638863 GSM7330663 GSM7330663 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000 SRX20314455 GSM7330664_r1 SRP437492 PRJNA971941 SRS17638864 GSM7330664 GSM7330664 RNA-Seq TRANSCRIPTOMIC cDNA RNA was isolated by means of the RNeasy Micro kit following manufacturer's instructions (Qiagen). Per sample, an amount of 100pg or 2ng of total RNA was used as input for the SMART-Seq v4 PLUS protocol to generate full-length cDNA (version “011821”) from Takara Bio USA, Inc. Subsequently, 3ng of purified double-stranded cDNA is enzymatically fragmented and stem-loop adapters ligated. Libraries are then amplified and indexed, generating Illumina-compatible libraries with unique dual indexes (UDIs) according to the manufacturer's protocol. Sequence-libraries of each sample were finally equimolarly pooled and sequenced on NovaSeq6000 using the Xp workflow, v1.5 kits, single read (100-8-8-0) at the VIB Nucleomics Core (www.nucleomics.be). Illumina NovaSeq 6000