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All these wheat bZIP genes were designated as TabZIP genes and given a number designation from 1 to 182 as an unique identifier as proposed for bZIP transcription factors in Arabidopsis [ 1].
The genes were designated NnAGPL1, NnAGPL2, and NnAGPS.
Four tuna CaM genes were designated as A to D according to the affinity with medaka CaM genes.
For analysis with Ingenuity, these genes, were designated as focus genes and were overlaid onto a global molecular network developed from information contained in the Ingenuity knowledge base.
Finally, to select for statistically significant changes, genes were designated as 'differentially expressed' if the corresponding ratios varied by at least 2-fold in at least 2 out of 56 samples (consistent with recommended criteria [67], [68]).
Genes were designated to be significantly differentially expressed if the p value was <0.001, and there was at least a 1.5-fold change in sequence counts between the two libraries.
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These genes are designated Systemic RNAi Defective, or SID.
These genes are designated APOBEC3A to APOBEC3H.
This genome with two WT fiber genes was designated Ad5/WT-fiber/E1 WT-fiber.
These genes are designated Dpu_Fer3HCH-1 to Dpu_Fer3HCH-5.
Hereafter, these methyltransferase genes are designated 'M.PabI homologs'.
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