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Neo-enthesis production and organization were analyzed using two histological scales.
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Therefore, the exon/intron organizations of all the MAPK cascade genes in cucumber were analyzed using the Gene Structure Display Server.
For this purpose, the structure and organization of all the available his genes that underwent fusion event(s) were analyzed using statistical and bioinformatics methods.
Interview transcripts were analyzed using content analysis in which data were coded using a hierarchical organization of codes.
Initially, the cDNA sequence and corresponding genomic sequence were analyzed using the Spidey software (http://www.ncbi.nlm.nih.gov/spidey) in order to establish the exon intron organization.
Images were analyzed using Gap Light Analyzer41.
Data were analyzed using one-way ANOVA.
Data were analyzed using Prism 5.0 (GraphPad Software).
Plates were analyzed using a Molecular Devices ImageXpress High-Content Analysis SysteMolecular Devices ImageXpress High-Content
Differentially expressed genes were analyzed using edgeR54.
Data were analyzed using GraphPad Prism version 6.0 (RRID:SCR_015807).
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