The resulting cDNA libraries were submitted to the University of Maryland Institute for Bioscience and Biotechnology Research (UM-IBBR) Sequencing Facility located at the University of Maryland—College Park. Sequencing data in the Sanger FastQ format were generated using an Illumina HiSeq 1500 system in rapid-run mode (100-nucleotide [nt], single-end reads). Biological triplicates were sequenced for each time point.
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