SRX4559166 Bd38R3 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676087 Bactrocera dorsalis at 38 degree celsius replicate 3 Bd38R3 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559167 Bd25R1 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676069 Bactrocera dorsalis at 25 degree celsius replicate 1 Bd25R1 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559168 Bd25R2 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676068 Bactrocera dorsalis at 25 degree celsius replicate 2 Bd25R2 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559169 Bd25R3 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676076 Bactrocera dorsalis at 25 degree celsius replicate 3 Bd25R3 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559170 Bd35R2 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676070 Bactrocera dorsalis at 35 degree celsius replicate 2 Bd35R2 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559171 Bd35R3 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676071 Bactrocera dorsalis at 35 degree celsius replicate 3 Bd35R3 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559172 Bd38R1 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676072 Bactrocera dorsalis at 38 degree celsius replicate 1 Bd38R1 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559173 Bd38R2 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676073 Bactrocera dorsalis at 38 degree celsius replicate 2 Bd38R2 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559174 Bc25R1 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676074 Bactrocera correcta at 25 degree celsius replicate 1 Bc25R1 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559175 Bc25R2 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676075 Bactrocera correcta at 25 degree celsius replicate 2 Bc25R2 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559176 Bc38R2 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676078 Bactrocera correcta at 38 degree celsius replicate 2 Bc38R2 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559177 Bc38R3 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676077 Bactrocera correcta at 38 degree celsius replicate 3 Bc38R3 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559178 Bc35R3 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676079 Bactrocera correcta at 35 degree celsius replicate 3 Bc35R3 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559179 Bc38R1 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676081 Bactrocera correcta at 38 degree celsius replicate 1 Bc38R1 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559180 Bc35R1 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676082 Bactrocera correcta at 35 degree celsius replicate 1 Bc35R1 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559181 Bc35R2 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676080 Bactrocera correcta at 35 degree celsius replicate 2 Bc35R2 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559182 Bc25R3 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676083 Bactrocera correcta at 25 degree celsius replicate 3 Bc25R3 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000 SRX4559183 Bd35R1 SRP158095 bp0 We extracted RNA from three groups of thirty larvae after exposing to specific temperatures (25C, 35C and 38C) for 4h followed by 25 C for 1 h. The quantity and integrity of the RNA were assessed with a Qubit RNA Assay Kit in Qubit2.0 Flurometer (Life Technologies, CA, USA) and an RNA Nano 6000 Assay Kit of the Agilent Bioanalyzer 2100 system (Agilent Technologies, CA, USA). All libraries ware prepared using NEBNextUltra RNA Library Prep Kit for Illumina (NEB, USA) according to the manufacturers protocol and were sequenced at the Biomarker Technologies company (Beijing, China). The clustering of index-coded samples was performed on a cBot Cluster Generation System using TruSeq PE Cluster Kit v3-cBot-HS (Illumina) and paired-end reads were generated through sequencing and the library preparations on an Illumina Hiseq 2000 platform after cluster generation. SRS3676084 Bactrocera dorsalis at 35 degree celsius replicate 1 Bd35R1 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2000