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For each sample (16, 55, 60, 21 are the ID number of samples in the file name) there are F1 and F2 since the sequencing was 100 bp paired-end. 2. The final heater tissue transcriptome and relative statistics. The raw reads were treated as follows: sequencing raw reads were submitted to a conservative pipeline of quality control (Fastqc, Trimmomatic, Rcorrector and Centrifuge). In the end of pre-processing stage, only raw reads with phred score ≥ 28 were kept for downstream analysis. The de-novo transcriptome assembly was built with the Trinity assembler (default parameters) and decontaminated using previously stablished methods (Machado <i>et al.</i>, 2019). 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