SRX23555814 EILTSA01 SRP488547 bp0 RNA concentration was measured on a NanoDrop 2000c spectrophotometer (Thermo Scientific, Thermo Fisher Scientific, Waltham, MA, USA), and RNA integrity (RIN 8.5) was evaluated on an Agilent 2100 Bioanalyzer using an RNA 6000 Nanokit (Agilent Technologies, Santa Clara, CA, USA). Finally, high-quality RNAs were processed with the TruSeq RNA Sample Prep Kit version 2.0 (Illumina). To identify reads from each sample, once the sequencing run was performed, each library was independently labelled with a specific multiplexing index (Illumina, San Diego, CA). The RNA-seq libraries were generated and sequenced in the Massive Sequencing Unit of the Instituto de Ecologa A.C. (INECOL, Veracruz, Mexico) using NextSeq500 platform (Illumina, San Diego, CA) and 2 150 bp paired-end reads format. SRS20402243 EILTSA01 EILTSA01 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX23555815 EILTSA02 SRP488547 bp0 RNA concentration was measured on a NanoDrop 2000c spectrophotometer (Thermo Scientific, Thermo Fisher Scientific, Waltham, MA, USA), and RNA integrity (RIN 8.5) was evaluated on an Agilent 2100 Bioanalyzer using an RNA 6000 Nanokit (Agilent Technologies, Santa Clara, CA, USA). Finally, high-quality RNAs were processed with the TruSeq RNA Sample Prep Kit version 2.0 (Illumina). To identify reads from each sample, once the sequencing run was performed, each library was independently labelled with a specific multiplexing index (Illumina, San Diego, CA). The RNA-seq libraries were generated and sequenced in the Massive Sequencing Unit of the Instituto de Ecologa A.C. (INECOL, Veracruz, Mexico) using NextSeq500 platform (Illumina, San Diego, CA) and 2 150 bp paired-end reads format. SRS20402245 EILTSA02 EILTSA02 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX23555816 EILTSA11 SRP488547 bp0 RNA concentration was measured on a NanoDrop 2000c spectrophotometer (Thermo Scientific, Thermo Fisher Scientific, Waltham, MA, USA), and RNA integrity (RIN 8.5) was evaluated on an Agilent 2100 Bioanalyzer using an RNA 6000 Nanokit (Agilent Technologies, Santa Clara, CA, USA). Finally, high-quality RNAs were processed with the TruSeq RNA Sample Prep Kit version 2.0 (Illumina). To identify reads from each sample, once the sequencing run was performed, each library was independently labelled with a specific multiplexing index (Illumina, San Diego, CA). The RNA-seq libraries were generated and sequenced in the Massive Sequencing Unit of the Instituto de Ecologa A.C. (INECOL, Veracruz, Mexico) using NextSeq500 platform (Illumina, San Diego, CA) and 2 150 bp paired-end reads format. SRS20402244 EILTSA11 EILTSA11 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX23555817 EILTSA12 SRP488547 bp0 RNA concentration was measured on a NanoDrop 2000c spectrophotometer (Thermo Scientific, Thermo Fisher Scientific, Waltham, MA, USA), and RNA integrity (RIN 8.5) was evaluated on an Agilent 2100 Bioanalyzer using an RNA 6000 Nanokit (Agilent Technologies, Santa Clara, CA, USA). Finally, high-quality RNAs were processed with the TruSeq RNA Sample Prep Kit version 2.0 (Illumina). To identify reads from each sample, once the sequencing run was performed, each library was independently labelled with a specific multiplexing index (Illumina, San Diego, CA). The RNA-seq libraries were generated and sequenced in the Massive Sequencing Unit of the Instituto de Ecologa A.C. (INECOL, Veracruz, Mexico) using NextSeq500 platform (Illumina, San Diego, CA) and 2 150 bp paired-end reads format. SRS20402246 EILTSA12 EILTSA12 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX23555818 EILTSA03 SRP488547 bp0 RNA concentration was measured on a NanoDrop 2000c spectrophotometer (Thermo Scientific, Thermo Fisher Scientific, Waltham, MA, USA), and RNA integrity (RIN 8.5) was evaluated on an Agilent 2100 Bioanalyzer using an RNA 6000 Nanokit (Agilent Technologies, Santa Clara, CA, USA). Finally, high-quality RNAs were processed with the TruSeq RNA Sample Prep Kit version 2.0 (Illumina). To identify reads from each sample, once the sequencing run was performed, each library was independently labelled with a specific multiplexing index (Illumina, San Diego, CA). The RNA-seq libraries were generated and sequenced in the Massive Sequencing Unit of the Instituto de Ecologa A.C. (INECOL, Veracruz, Mexico) using NextSeq500 platform (Illumina, San Diego, CA) and 2 150 bp paired-end reads format. SRS20402247 EILTSA03 EILTSA03 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX23555819 EILTSA04 SRP488547 bp0 RNA concentration was measured on a NanoDrop 2000c spectrophotometer (Thermo Scientific, Thermo Fisher Scientific, Waltham, MA, USA), and RNA integrity (RIN 8.5) was evaluated on an Agilent 2100 Bioanalyzer using an RNA 6000 Nanokit (Agilent Technologies, Santa Clara, CA, USA). Finally, high-quality RNAs were processed with the TruSeq RNA Sample Prep Kit version 2.0 (Illumina). To identify reads from each sample, once the sequencing run was performed, each library was independently labelled with a specific multiplexing index (Illumina, San Diego, CA). The RNA-seq libraries were generated and sequenced in the Massive Sequencing Unit of the Instituto de Ecologa A.C. (INECOL, Veracruz, Mexico) using NextSeq500 platform (Illumina, San Diego, CA) and 2 150 bp paired-end reads format. SRS20402248 EILTSA04 EILTSA04 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX23555820 EILTSA05 SRP488547 bp0 RNA concentration was measured on a NanoDrop 2000c spectrophotometer (Thermo Scientific, Thermo Fisher Scientific, Waltham, MA, USA), and RNA integrity (RIN 8.5) was evaluated on an Agilent 2100 Bioanalyzer using an RNA 6000 Nanokit (Agilent Technologies, Santa Clara, CA, USA). Finally, high-quality RNAs were processed with the TruSeq RNA Sample Prep Kit version 2.0 (Illumina). To identify reads from each sample, once the sequencing run was performed, each library was independently labelled with a specific multiplexing index (Illumina, San Diego, CA). The RNA-seq libraries were generated and sequenced in the Massive Sequencing Unit of the Instituto de Ecologa A.C. (INECOL, Veracruz, Mexico) using NextSeq500 platform (Illumina, San Diego, CA) and 2 150 bp paired-end reads format. SRS20402249 EILTSA05 EILTSA05 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX23555821 EILTSA06 SRP488547 bp0 RNA concentration was measured on a NanoDrop 2000c spectrophotometer (Thermo Scientific, Thermo Fisher Scientific, Waltham, MA, USA), and RNA integrity (RIN 8.5) was evaluated on an Agilent 2100 Bioanalyzer using an RNA 6000 Nanokit (Agilent Technologies, Santa Clara, CA, USA). Finally, high-quality RNAs were processed with the TruSeq RNA Sample Prep Kit version 2.0 (Illumina). To identify reads from each sample, once the sequencing run was performed, each library was independently labelled with a specific multiplexing index (Illumina, San Diego, CA). The RNA-seq libraries were generated and sequenced in the Massive Sequencing Unit of the Instituto de Ecologa A.C. (INECOL, Veracruz, Mexico) using NextSeq500 platform (Illumina, San Diego, CA) and 2 150 bp paired-end reads format. SRS20402250 EILTSA06 EILTSA06 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX23555822 EILTSA07 SRP488547 bp0 RNA concentration was measured on a NanoDrop 2000c spectrophotometer (Thermo Scientific, Thermo Fisher Scientific, Waltham, MA, USA), and RNA integrity (RIN 8.5) was evaluated on an Agilent 2100 Bioanalyzer using an RNA 6000 Nanokit (Agilent Technologies, Santa Clara, CA, USA). Finally, high-quality RNAs were processed with the TruSeq RNA Sample Prep Kit version 2.0 (Illumina). To identify reads from each sample, once the sequencing run was performed, each library was independently labelled with a specific multiplexing index (Illumina, San Diego, CA). The RNA-seq libraries were generated and sequenced in the Massive Sequencing Unit of the Instituto de Ecologa A.C. (INECOL, Veracruz, Mexico) using NextSeq500 platform (Illumina, San Diego, CA) and 2 150 bp paired-end reads format. SRS20402252 EILTSA07 EILTSA07 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX23555823 EILTSA08 SRP488547 bp0 RNA concentration was measured on a NanoDrop 2000c spectrophotometer (Thermo Scientific, Thermo Fisher Scientific, Waltham, MA, USA), and RNA integrity (RIN 8.5) was evaluated on an Agilent 2100 Bioanalyzer using an RNA 6000 Nanokit (Agilent Technologies, Santa Clara, CA, USA). Finally, high-quality RNAs were processed with the TruSeq RNA Sample Prep Kit version 2.0 (Illumina). To identify reads from each sample, once the sequencing run was performed, each library was independently labelled with a specific multiplexing index (Illumina, San Diego, CA). The RNA-seq libraries were generated and sequenced in the Massive Sequencing Unit of the Instituto de Ecologa A.C. (INECOL, Veracruz, Mexico) using NextSeq500 platform (Illumina, San Diego, CA) and 2 150 bp paired-end reads format. SRS20402251 EILTSA08 EILTSA08 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX23555824 EILTSA09 SRP488547 bp0 RNA concentration was measured on a NanoDrop 2000c spectrophotometer (Thermo Scientific, Thermo Fisher Scientific, Waltham, MA, USA), and RNA integrity (RIN 8.5) was evaluated on an Agilent 2100 Bioanalyzer using an RNA 6000 Nanokit (Agilent Technologies, Santa Clara, CA, USA). Finally, high-quality RNAs were processed with the TruSeq RNA Sample Prep Kit version 2.0 (Illumina). To identify reads from each sample, once the sequencing run was performed, each library was independently labelled with a specific multiplexing index (Illumina, San Diego, CA). The RNA-seq libraries were generated and sequenced in the Massive Sequencing Unit of the Instituto de Ecologa A.C. (INECOL, Veracruz, Mexico) using NextSeq500 platform (Illumina, San Diego, CA) and 2 150 bp paired-end reads format. SRS20402253 EILTSA09 EILTSA09 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500 SRX23555825 EILTSA10 SRP488547 bp0 RNA concentration was measured on a NanoDrop 2000c spectrophotometer (Thermo Scientific, Thermo Fisher Scientific, Waltham, MA, USA), and RNA integrity (RIN 8.5) was evaluated on an Agilent 2100 Bioanalyzer using an RNA 6000 Nanokit (Agilent Technologies, Santa Clara, CA, USA). Finally, high-quality RNAs were processed with the TruSeq RNA Sample Prep Kit version 2.0 (Illumina). To identify reads from each sample, once the sequencing run was performed, each library was independently labelled with a specific multiplexing index (Illumina, San Diego, CA). The RNA-seq libraries were generated and sequenced in the Massive Sequencing Unit of the Instituto de Ecologa A.C. (INECOL, Veracruz, Mexico) using NextSeq500 platform (Illumina, San Diego, CA) and 2 150 bp paired-end reads format. SRS20402254 EILTSA10 EILTSA10 RNA-Seq TRANSCRIPTOMIC RANDOM NextSeq 500