SRX3395770 XJOVA_20151015_K00134_IL100062652_S25 SRP125059 bp0 RNA samples were analyzed for quantity and quality using an Agilent 2100 Bioanalyzer with the RNA 6000 Nano Kit. Samples with a RIN greater than 9.0 were sent to the Institute for Genome Sciences (University of Maryland School of Medicine) for RNA-Seq using the Illumina HiSeq4000 platform with 150 bp, paired-end sequencing. RNA-seq libraries were prepared using the TruSeq RNA Sample Prep Kit (Illumina, San Diego, CA). Double-stranded cDNA was ligated to seven indexed nucleotide adapters and purified between enzymatic reactions. Library size selection was performed using SPRIselect beads (Beckman Coulter Genomics, Danvers, MA). SRS2689953 0HourHemolymphS3 XJOVA_20151015_K00134_IL100062652_S25 RNA-Seq TRANSCRIPTOMIC Oligo-dT Illumina HiSeq 4000 SRX3395771 XJOVA_20151015_K00134_IL100062653_S26 SRP125059 bp0 RNA samples were analyzed for quantity and quality using an Agilent 2100 Bioanalyzer with the RNA 6000 Nano Kit. Samples with a RIN greater than 9.0 were sent to the Institute for Genome Sciences (University of Maryland School of Medicine) for RNA-Seq using the Illumina HiSeq4000 platform with 150 bp, paired-end sequencing. RNA-seq libraries were prepared using the TruSeq RNA Sample Prep Kit (Illumina, San Diego, CA). Double-stranded cDNA was ligated to seven indexed nucleotide adapters and purified between enzymatic reactions. Library size selection was performed using SPRIselect beads (Beckman Coulter Genomics, Danvers, MA). SRS2689954 9HourHemolymphS1 XJOVA_20151015_K00134_IL100062653_S26 RNA-Seq TRANSCRIPTOMIC Oligo-dT Illumina HiSeq 4000 SRX3395772 XJOVA_20151015_K00134_IL100062650_S23 SRP125059 bp0 RNA samples were analyzed for quantity and quality using an Agilent 2100 Bioanalyzer with the RNA 6000 Nano Kit. Samples with a RIN greater than 9.0 were sent to the Institute for Genome Sciences (University of Maryland School of Medicine) for RNA-Seq using the Illumina HiSeq4000 platform with 150 bp, paired-end sequencing. RNA-seq libraries were prepared using the TruSeq RNA Sample Prep Kit (Illumina, San Diego, CA). Double-stranded cDNA was ligated to seven indexed nucleotide adapters and purified between enzymatic reactions. Library size selection was performed using SPRIselect beads (Beckman Coulter Genomics, Danvers, MA). SRS2689955 0HourHemolymphS1 XJOVA_20151015_K00134_IL100062650_S23 RNA-Seq TRANSCRIPTOMIC Oligo-dT Illumina HiSeq 4000 SRX3395773 XJOVA_20151015_K00134_IL100062651_S24 SRP125059 bp0 RNA samples were analyzed for quantity and quality using an Agilent 2100 Bioanalyzer with the RNA 6000 Nano Kit. Samples with a RIN greater than 9.0 were sent to the Institute for Genome Sciences (University of Maryland School of Medicine) for RNA-Seq using the Illumina HiSeq4000 platform with 150 bp, paired-end sequencing. RNA-seq libraries were prepared using the TruSeq RNA Sample Prep Kit (Illumina, San Diego, CA). Double-stranded cDNA was ligated to seven indexed nucleotide adapters and purified between enzymatic reactions. Library size selection was performed using SPRIselect beads (Beckman Coulter Genomics, Danvers, MA). SRS2689956 0HourHemolymphS2 XJOVA_20151015_K00134_IL100062651_S24 RNA-Seq TRANSCRIPTOMIC Oligo-dT Illumina HiSeq 4000 SRX3395774 XJOVA_20151015_K00134_IL100062654_S27 SRP125059 bp0 RNA samples were analyzed for quantity and quality using an Agilent 2100 Bioanalyzer with the RNA 6000 Nano Kit. Samples with a RIN greater than 9.0 were sent to the Institute for Genome Sciences (University of Maryland School of Medicine) for RNA-Seq using the Illumina HiSeq4000 platform with 150 bp, paired-end sequencing. RNA-seq libraries were prepared using the TruSeq RNA Sample Prep Kit (Illumina, San Diego, CA). Double-stranded cDNA was ligated to seven indexed nucleotide adapters and purified between enzymatic reactions. Library size selection was performed using SPRIselect beads (Beckman Coulter Genomics, Danvers, MA). SRS2689957 9HourHemolymphS2 XJOVA_20151015_K00134_IL100062654_S27 RNA-Seq TRANSCRIPTOMIC Oligo-dT Illumina HiSeq 4000 SRX3395775 XJOVA_20151015_K00134_IL100062657_S28 SRP125059 bp0 RNA samples were analyzed for quantity and quality using an Agilent 2100 Bioanalyzer with the RNA 6000 Nano Kit. Samples with a RIN greater than 9.0 were sent to the Institute for Genome Sciences (University of Maryland School of Medicine) for RNA-Seq using the Illumina HiSeq4000 platform with 150 bp, paired-end sequencing. RNA-seq libraries were prepared using the TruSeq RNA Sample Prep Kit (Illumina, San Diego, CA). Double-stranded cDNA was ligated to seven indexed nucleotide adapters and purified between enzymatic reactions. Library size selection was performed using SPRIselect beads (Beckman Coulter Genomics, Danvers, MA). SRS2689958 9HourHemolymphS3 XJOVA_20151015_K00134_IL100062657_S28 RNA-Seq TRANSCRIPTOMIC Oligo-dT Illumina HiSeq 4000