SRX15039547 GSM6071590_r1 SRP372689 PRJNA833056 SRS12786173 GSM6071590 GSM6071590 RNA-Seq TRANSCRIPTOMIC cDNA RNA and gDNA fractions from stage 16 medaka embryos were extracted using TRIzol (Ambion). Possible DNA contamination was eliminated treating the RNA samples with TURBO DNAse-free (Ambion). Each embryo was genotyped using its DNA fraction following a previously published approach (Vázquez-Marín et al., 2019). RNA from embryos with the same genotype were pooled together in up to four replicates and sent to sequence (Illumina Hiseq 2500). cDNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2500 SRX15039548 GSM6071591_r1 SRP372689 PRJNA833056 SRS12786175 GSM6071591 GSM6071591 RNA-Seq TRANSCRIPTOMIC cDNA RNA and gDNA fractions from stage 16 medaka embryos were extracted using TRIzol (Ambion). Possible DNA contamination was eliminated treating the RNA samples with TURBO DNAse-free (Ambion). Each embryo was genotyped using its DNA fraction following a previously published approach (Vázquez-Marín et al., 2019). RNA from embryos with the same genotype were pooled together in up to four replicates and sent to sequence (Illumina Hiseq 2500). cDNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2500 SRX15039549 GSM6071592_r1 SRP372689 PRJNA833056 SRS12786174 GSM6071592 GSM6071592 RNA-Seq TRANSCRIPTOMIC cDNA RNA and gDNA fractions from stage 16 medaka embryos were extracted using TRIzol (Ambion). Possible DNA contamination was eliminated treating the RNA samples with TURBO DNAse-free (Ambion). Each embryo was genotyped using its DNA fraction following a previously published approach (Vázquez-Marín et al., 2019). RNA from embryos with the same genotype were pooled together in up to four replicates and sent to sequence (Illumina Hiseq 2500). cDNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2500 SRX15039550 GSM6071593_r1 SRP372689 PRJNA833056 SRS12786183 GSM6071593 GSM6071593 RNA-Seq TRANSCRIPTOMIC cDNA RNA and gDNA fractions from stage 16 medaka embryos were extracted using TRIzol (Ambion). Possible DNA contamination was eliminated treating the RNA samples with TURBO DNAse-free (Ambion). Each embryo was genotyped using its DNA fraction following a previously published approach (Vázquez-Marín et al., 2019). RNA from embryos with the same genotype were pooled together in up to four replicates and sent to sequence (Illumina Hiseq 2500). cDNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2500 SRX15039551 GSM6071594_r1 SRP372689 PRJNA833056 SRS12786176 GSM6071594 GSM6071594 RNA-Seq TRANSCRIPTOMIC cDNA RNA and gDNA fractions from stage 16 medaka embryos were extracted using TRIzol (Ambion). Possible DNA contamination was eliminated treating the RNA samples with TURBO DNAse-free (Ambion). Each embryo was genotyped using its DNA fraction following a previously published approach (Vázquez-Marín et al., 2019). RNA from embryos with the same genotype were pooled together in up to four replicates and sent to sequence (Illumina Hiseq 2500). cDNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2500 SRX15039552 GSM6071595_r1 SRP372689 PRJNA833056 SRS12786177 GSM6071595 GSM6071595 RNA-Seq TRANSCRIPTOMIC cDNA RNA and gDNA fractions from stage 16 medaka embryos were extracted using TRIzol (Ambion). Possible DNA contamination was eliminated treating the RNA samples with TURBO DNAse-free (Ambion). Each embryo was genotyped using its DNA fraction following a previously published approach (Vázquez-Marín et al., 2019). RNA from embryos with the same genotype were pooled together in up to four replicates and sent to sequence (Illumina Hiseq 2500). cDNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2500 SRX15039553 GSM6071596_r1 SRP372689 PRJNA833056 SRS12786178 GSM6071596 GSM6071596 RNA-Seq TRANSCRIPTOMIC cDNA RNA and gDNA fractions from stage 16 medaka embryos were extracted using TRIzol (Ambion). Possible DNA contamination was eliminated treating the RNA samples with TURBO DNAse-free (Ambion). Each embryo was genotyped using its DNA fraction following a previously published approach (Vázquez-Marín et al., 2019). RNA from embryos with the same genotype were pooled together in up to four replicates and sent to sequence (Illumina Hiseq 2500). cDNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2500 SRX15039554 GSM6071597_r1 SRP372689 PRJNA833056 SRS12786179 GSM6071597 GSM6071597 RNA-Seq TRANSCRIPTOMIC cDNA RNA and gDNA fractions from stage 16 medaka embryos were extracted using TRIzol (Ambion). Possible DNA contamination was eliminated treating the RNA samples with TURBO DNAse-free (Ambion). Each embryo was genotyped using its DNA fraction following a previously published approach (Vázquez-Marín et al., 2019). RNA from embryos with the same genotype were pooled together in up to four replicates and sent to sequence (Illumina Hiseq 2500). cDNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2500 SRX15039555 GSM6071598_r1 SRP372689 PRJNA833056 SRS12786180 GSM6071598 GSM6071598 RNA-Seq TRANSCRIPTOMIC cDNA RNA and gDNA fractions from stage 16 medaka embryos were extracted using TRIzol (Ambion). Possible DNA contamination was eliminated treating the RNA samples with TURBO DNAse-free (Ambion). Each embryo was genotyped using its DNA fraction following a previously published approach (Vázquez-Marín et al., 2019). RNA from embryos with the same genotype were pooled together in up to four replicates and sent to sequence (Illumina Hiseq 2500). cDNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2500 SRX15039556 GSM6071599_r1 SRP372689 PRJNA833056 SRS12786181 GSM6071599 GSM6071599 RNA-Seq TRANSCRIPTOMIC cDNA RNA and gDNA fractions from stage 16 medaka embryos were extracted using TRIzol (Ambion). Possible DNA contamination was eliminated treating the RNA samples with TURBO DNAse-free (Ambion). Each embryo was genotyped using its DNA fraction following a previously published approach (Vázquez-Marín et al., 2019). RNA from embryos with the same genotype were pooled together in up to four replicates and sent to sequence (Illumina Hiseq 2500). cDNA libraries were prepared for sequencing using standard Illumina protocols. Illumina HiSeq 2500