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Samples from the six biological replicates were spread across different slides, Cy3 fluorescence content (dye incorporation rate × volume) was also taken into consideration.
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The probe intensities from various biological replicates were normalized using scale normalization using median absolute deviation as a spread measure.
At least two biological replicates were performed.
Four biological replicates were performed for each studied condition.
Three biological replicates were used for each treatment or control.
Two biological replicates were prepared for each ChIP target.
Three biological replicates were collected for each stage.
Three biological replicates were collected at the same time.
Four biological replicates were performed per test condition, including controls.
Biological replicates were then merged using samtools (Version 1.4).
Three biological replicates were used for diploid tissue, and five biological replicates were used for A. hypogaea cv.
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