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. 2020 Dec 2;13:587815. doi: 10.3389/fnmol.2020.587815

FIGURE 1.

FIGURE 1

Transcriptome study experimental schedule. Spontaneous development and effects of HI were studied in parallel. Cy3 signals were used for development study at P5 and P10. mRNA extraction amplification and labeling. Co-hybridization of Cy3 labeled P2 and Cy5-P15 samples. Co-hybridization of Cy3-naïve and Cy5-HI samples at P5 or P10. Signal filtering on signal quality and basal expression at the same thresholds. Extraction of HI effects at P5 or P10 using a GeneSpring® two-color procedure. Extraction of ontogenetic variations between P2, P5, P10, and P15 using a GeneSpring® one-color procedure. Biostatistical analyses of HI effects at P5 or P10 utilizing DAVID®, Revigo®, and IPA®. Identification of convergences between spontaneous development and effects of HI at P5 or P10 using Excel and GraphPad. cRNA: Cy3 or Cy5 labeled complementary RNA from retro-transcribed DNA obtained from extracted mRNA.