GSM7151704: WT RG_rep1; Drosophila melanogaster; RNA-Seq

SRX19888171 GSM7151704_r1 GSM7151704: WT RG_rep1; Drosophila melanogaster; RNA-Seq SRP431191 PRJNA952685 SRS17242228 GSM7151704 GSM7151704 RNA-Seq TRANSCRIPTOMIC cDNA Trizol extraction of total RNA from dissected ring glands was performed according to manufacturer's instructions. Animals were matched by developmental stage of wandering third instar larva. n = 80 ring glands per replicate. Total RNA was submitted to Novogene for library construction and sequencing. At Novogene, polyA enrichment was performed to prepare mRNA libraries. Libraries were evaluated for quality using the Agilent Bioanalyzer 2100 system. Sequencing was performed on an Illumina NovaSeq PE150 sequencing platform (2 x 150bp) cycles. Illumina NovaSeq 6000 SRX19888172 GSM7151705_r1 GSM7151705: WT RG_rep2; Drosophila melanogaster; RNA-Seq SRP431191 PRJNA952685 SRS17242229 GSM7151705 GSM7151705 RNA-Seq TRANSCRIPTOMIC cDNA Trizol extraction of total RNA from dissected ring glands was performed according to manufacturer's instructions. Animals were matched by developmental stage of wandering third instar larva. n = 80 ring glands per replicate. Total RNA was submitted to Novogene for library construction and sequencing. At Novogene, polyA enrichment was performed to prepare mRNA libraries. Libraries were evaluated for quality using the Agilent Bioanalyzer 2100 system. Sequencing was performed on an Illumina NovaSeq PE150 sequencing platform (2 x 150bp) cycles. Illumina NovaSeq 6000 SRX19888173 GSM7151706_r1 GSM7151706: WT RG_rep3; Drosophila melanogaster; RNA-Seq SRP431191 PRJNA952685 SRS17242230 GSM7151706 GSM7151706 RNA-Seq TRANSCRIPTOMIC cDNA Trizol extraction of total RNA from dissected ring glands was performed according to manufacturer's instructions. Animals were matched by developmental stage of wandering third instar larva. n = 80 ring glands per replicate. Total RNA was submitted to Novogene for library construction and sequencing. At Novogene, polyA enrichment was performed to prepare mRNA libraries. Libraries were evaluated for quality using the Agilent Bioanalyzer 2100 system. Sequencing was performed on an Illumina NovaSeq PE150 sequencing platform (2 x 150bp) cycles. Illumina NovaSeq 6000 SRX19888174 GSM7151707_r1 GSM7151707: WT RG_rep4; Drosophila melanogaster; RNA-Seq SRP431191 PRJNA952685 SRS17242231 GSM7151707 GSM7151707 RNA-Seq TRANSCRIPTOMIC cDNA Trizol extraction of total RNA from dissected ring glands was performed according to manufacturer's instructions. Animals were matched by developmental stage of wandering third instar larva. n = 80 ring glands per replicate. Total RNA was submitted to Novogene for library construction and sequencing. At Novogene, polyA enrichment was performed to prepare mRNA libraries. Libraries were evaluated for quality using the Agilent Bioanalyzer 2100 system. Sequencing was performed on an Illumina NovaSeq PE150 sequencing platform (2 x 150bp) cycles. Illumina NovaSeq 6000 SRX19888175 GSM7151708_r1 GSM7151708: kdm5[140] RG_rep1; Drosophila melanogaster; RNA-Seq SRP431191 PRJNA952685 SRS17242232 GSM7151708 GSM7151708 RNA-Seq TRANSCRIPTOMIC cDNA Trizol extraction of total RNA from dissected ring glands was performed according to manufacturer's instructions. Animals were matched by developmental stage of wandering third instar larva. n = 80 ring glands per replicate. Total RNA was submitted to Novogene for library construction and sequencing. At Novogene, polyA enrichment was performed to prepare mRNA libraries. Libraries were evaluated for quality using the Agilent Bioanalyzer 2100 system. Sequencing was performed on an Illumina NovaSeq PE150 sequencing platform (2 x 150bp) cycles. Illumina NovaSeq 6000 SRX19888176 GSM7151709_r1 GSM7151709: kdm5[140] RG_rep2; Drosophila melanogaster; RNA-Seq SRP431191 PRJNA952685 SRS17242233 GSM7151709 GSM7151709 RNA-Seq TRANSCRIPTOMIC cDNA Trizol extraction of total RNA from dissected ring glands was performed according to manufacturer's instructions. Animals were matched by developmental stage of wandering third instar larva. n = 80 ring glands per replicate. Total RNA was submitted to Novogene for library construction and sequencing. At Novogene, polyA enrichment was performed to prepare mRNA libraries. Libraries were evaluated for quality using the Agilent Bioanalyzer 2100 system. Sequencing was performed on an Illumina NovaSeq PE150 sequencing platform (2 x 150bp) cycles. Illumina NovaSeq 6000 SRX19888177 GSM7151710_r1 GSM7151710: kdm5[140] RG_rep3; Drosophila melanogaster; RNA-Seq SRP431191 PRJNA952685 SRS17242234 GSM7151710 GSM7151710 RNA-Seq TRANSCRIPTOMIC cDNA Trizol extraction of total RNA from dissected ring glands was performed according to manufacturer's instructions. Animals were matched by developmental stage of wandering third instar larva. n = 80 ring glands per replicate. Total RNA was submitted to Novogene for library construction and sequencing. At Novogene, polyA enrichment was performed to prepare mRNA libraries. Libraries were evaluated for quality using the Agilent Bioanalyzer 2100 system. Sequencing was performed on an Illumina NovaSeq PE150 sequencing platform (2 x 150bp) cycles. Illumina NovaSeq 6000 SRX19888178 GSM7151711_r1 GSM7151711: kdm5[140] RG_rep4; Drosophila melanogaster; RNA-Seq SRP431191 PRJNA952685 SRS17242235 GSM7151711 GSM7151711 RNA-Seq TRANSCRIPTOMIC cDNA Trizol extraction of total RNA from dissected ring glands was performed according to manufacturer's instructions. Animals were matched by developmental stage of wandering third instar larva. n = 80 ring glands per replicate. Total RNA was submitted to Novogene for library construction and sequencing. At Novogene, polyA enrichment was performed to prepare mRNA libraries. Libraries were evaluated for quality using the Agilent Bioanalyzer 2100 system. Sequencing was performed on an Illumina NovaSeq PE150 sequencing platform (2 x 150bp) cycles. Illumina NovaSeq 6000