SRX18397895 GSM6758286_r1 SRP410238 PRJNA906091 SRS15881732 GSM6758286 GSM6758286 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish larvae from all groups groups (n=4) were resuspended and crushed in 0.5 ml of TRIzol Reagent The NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB #E7760S/L) was used to process the samples. Briefly, mRNA was isolated from total RNA using oligo-dT magnetic beads. After fragmentation of the mRNA, a cDNA synthesis was performed. This was used for ligation of the sequencing adapters and PCR amplification of the resulting product. The quality and yield after sample preparation was measured with Fragment Analyzer. The size of the resulting products was consistent with the expected size distribution (a broad peak between 300-500 bp). Illumina NovaSeq 6000 SRX18397896 GSM6758287_r1 SRP410238 PRJNA906091 SRS15881733 GSM6758287 GSM6758287 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish larvae from all groups groups (n=4) were resuspended and crushed in 0.5 ml of TRIzol Reagent The NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB #E7760S/L) was used to process the samples. Briefly, mRNA was isolated from total RNA using oligo-dT magnetic beads. After fragmentation of the mRNA, a cDNA synthesis was performed. This was used for ligation of the sequencing adapters and PCR amplification of the resulting product. The quality and yield after sample preparation was measured with Fragment Analyzer. The size of the resulting products was consistent with the expected size distribution (a broad peak between 300-500 bp). Illumina NovaSeq 6000 SRX18397897 GSM6758288_r1 SRP410238 PRJNA906091 SRS15881734 GSM6758288 GSM6758288 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish larvae from all groups groups (n=4) were resuspended and crushed in 0.5 ml of TRIzol Reagent The NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB #E7760S/L) was used to process the samples. Briefly, mRNA was isolated from total RNA using oligo-dT magnetic beads. After fragmentation of the mRNA, a cDNA synthesis was performed. This was used for ligation of the sequencing adapters and PCR amplification of the resulting product. The quality and yield after sample preparation was measured with Fragment Analyzer. The size of the resulting products was consistent with the expected size distribution (a broad peak between 300-500 bp). Illumina NovaSeq 6000 SRX18397898 GSM6758289_r1 SRP410238 PRJNA906091 SRS15881735 GSM6758289 GSM6758289 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish larvae from all groups groups (n=4) were resuspended and crushed in 0.5 ml of TRIzol Reagent The NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB #E7760S/L) was used to process the samples. Briefly, mRNA was isolated from total RNA using oligo-dT magnetic beads. After fragmentation of the mRNA, a cDNA synthesis was performed. This was used for ligation of the sequencing adapters and PCR amplification of the resulting product. The quality and yield after sample preparation was measured with Fragment Analyzer. The size of the resulting products was consistent with the expected size distribution (a broad peak between 300-500 bp). Illumina NovaSeq 6000 SRX18397899 GSM6758290_r1 SRP410238 PRJNA906091 SRS15881736 GSM6758290 GSM6758290 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish larvae from all groups groups (n=4) were resuspended and crushed in 0.5 ml of TRIzol Reagent The NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB #E7760S/L) was used to process the samples. Briefly, mRNA was isolated from total RNA using oligo-dT magnetic beads. After fragmentation of the mRNA, a cDNA synthesis was performed. This was used for ligation of the sequencing adapters and PCR amplification of the resulting product. The quality and yield after sample preparation was measured with Fragment Analyzer. The size of the resulting products was consistent with the expected size distribution (a broad peak between 300-500 bp). Illumina NovaSeq 6000 SRX18397900 GSM6758291_r1 SRP410238 PRJNA906091 SRS15881737 GSM6758291 GSM6758291 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish larvae from all groups groups (n=4) were resuspended and crushed in 0.5 ml of TRIzol Reagent The NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB #E7760S/L) was used to process the samples. Briefly, mRNA was isolated from total RNA using oligo-dT magnetic beads. After fragmentation of the mRNA, a cDNA synthesis was performed. This was used for ligation of the sequencing adapters and PCR amplification of the resulting product. The quality and yield after sample preparation was measured with Fragment Analyzer. The size of the resulting products was consistent with the expected size distribution (a broad peak between 300-500 bp). Illumina NovaSeq 6000 SRX18397901 GSM6758292_r1 SRP410238 PRJNA906091 SRS15881738 GSM6758292 GSM6758292 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish larvae from all groups groups (n=4) were resuspended and crushed in 0.5 ml of TRIzol Reagent The NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB #E7760S/L) was used to process the samples. Briefly, mRNA was isolated from total RNA using oligo-dT magnetic beads. After fragmentation of the mRNA, a cDNA synthesis was performed. This was used for ligation of the sequencing adapters and PCR amplification of the resulting product. The quality and yield after sample preparation was measured with Fragment Analyzer. The size of the resulting products was consistent with the expected size distribution (a broad peak between 300-500 bp). Illumina NovaSeq 6000 SRX18397902 GSM6758293_r1 SRP410238 PRJNA906091 SRS15881739 GSM6758293 GSM6758293 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish larvae from all groups groups (n=4) were resuspended and crushed in 0.5 ml of TRIzol Reagent The NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB #E7760S/L) was used to process the samples. Briefly, mRNA was isolated from total RNA using oligo-dT magnetic beads. After fragmentation of the mRNA, a cDNA synthesis was performed. This was used for ligation of the sequencing adapters and PCR amplification of the resulting product. The quality and yield after sample preparation was measured with Fragment Analyzer. The size of the resulting products was consistent with the expected size distribution (a broad peak between 300-500 bp). Illumina NovaSeq 6000 SRX18397903 GSM6758294_r1 SRP410238 PRJNA906091 SRS15881740 GSM6758294 GSM6758294 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish larvae from all groups groups (n=4) were resuspended and crushed in 0.5 ml of TRIzol Reagent The NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB #E7760S/L) was used to process the samples. Briefly, mRNA was isolated from total RNA using oligo-dT magnetic beads. After fragmentation of the mRNA, a cDNA synthesis was performed. This was used for ligation of the sequencing adapters and PCR amplification of the resulting product. The quality and yield after sample preparation was measured with Fragment Analyzer. The size of the resulting products was consistent with the expected size distribution (a broad peak between 300-500 bp). Illumina NovaSeq 6000 SRX18397904 GSM6758295_r1 SRP410238 PRJNA906091 SRS15881741 GSM6758295 GSM6758295 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish larvae from all groups groups (n=4) were resuspended and crushed in 0.5 ml of TRIzol Reagent The NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB #E7760S/L) was used to process the samples. Briefly, mRNA was isolated from total RNA using oligo-dT magnetic beads. After fragmentation of the mRNA, a cDNA synthesis was performed. This was used for ligation of the sequencing adapters and PCR amplification of the resulting product. The quality and yield after sample preparation was measured with Fragment Analyzer. The size of the resulting products was consistent with the expected size distribution (a broad peak between 300-500 bp). Illumina NovaSeq 6000 SRX18397905 GSM6758296_r1 SRP410238 PRJNA906091 SRS15881742 GSM6758296 GSM6758296 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish larvae from all groups groups (n=4) were resuspended and crushed in 0.5 ml of TRIzol Reagent The NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB #E7760S/L) was used to process the samples. Briefly, mRNA was isolated from total RNA using oligo-dT magnetic beads. After fragmentation of the mRNA, a cDNA synthesis was performed. This was used for ligation of the sequencing adapters and PCR amplification of the resulting product. The quality and yield after sample preparation was measured with Fragment Analyzer. The size of the resulting products was consistent with the expected size distribution (a broad peak between 300-500 bp). Illumina NovaSeq 6000 SRX18397906 GSM6758297_r1 SRP410238 PRJNA906091 SRS15881743 GSM6758297 GSM6758297 RNA-Seq TRANSCRIPTOMIC cDNA Zebrafish larvae from all groups groups (n=4) were resuspended and crushed in 0.5 ml of TRIzol Reagent The NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (NEB #E7760S/L) was used to process the samples. Briefly, mRNA was isolated from total RNA using oligo-dT magnetic beads. After fragmentation of the mRNA, a cDNA synthesis was performed. This was used for ligation of the sequencing adapters and PCR amplification of the resulting product. The quality and yield after sample preparation was measured with Fragment Analyzer. The size of the resulting products was consistent with the expected size distribution (a broad peak between 300-500 bp). Illumina NovaSeq 6000