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Differentially expressed genes were analyzed using edgeR54.
The pathway distributions of essential genes were analyzed via KEGG.
Sequences of all three chloroplast genes were analyzed in BioEdit 7.2.5.
This indicates that when fewer genes were analyzed, the TH index of tumor samples could have been calculated incorrectly.
After 48 hours, knockdown efficiency was confirmed by qRT-PCR, and then all the downstream genes were analyzed.
After 10 h of induction, the expression levels of these genes were analyzed.
Additionally, the gene structure and motif compositions of the apple NAC genes were analyzed.
Ten genes were analyzed and none were sensitive to peptide or fiber modulus in the absence of cyclic tensile strain.
The expression of cell cycle and apoptosis related genes were analyzed by quantitative RT-PCR and western blot.
The messenger RNAs from these tissues were used on complementary DNA expression arrays; 488 genes were analyzed.
The coding exons of 208 genes were analyzed in 453 patients with CAKUT using next-generation sequencing.
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