Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Total RNA was extracted using the Trizol (Invitrogen) procedure or RNAeasy/RNAeasy Lipid/miRNeasy (Qiagen) column purification kits. RNA quality was assessed using an Agilent 2100 Bioanalyzer. Strand‐specific (marmoset) and non-strand-specific (elephant) RNA-seq libraries were prepared according to the Directional mRNA‐seq Library Prep Pre‐Release Protocols from Illumina for male and female heart, liver, kidney, frontal cortex, cerebellum, ovary and testis (marmoset), and fibroblast (elephant). The testis samples for the common marmoset come from two different individuals. Marmoset tissues were obtained from the German Primate Center ("Deutsches Primatenzentrum") in Göttingen, Germany. Elephant fibroblasts were obtained from the Australian National University, Canberra, Australia. Each of these libraries were sequenced (101 cycles, single‐end) using the Illumina HiSeq 2000 platform, except for marmoset testis samples (individual 2) and both elephant fibroblast samples that were sequenced (79 cycles, single‐end) using the Illumina Illumina Genome Analyzer IIx platform.