Sentence examples for between samples were then from inspiring English sources
Relative expression levels between samples were then calculated as fold changes, where each PCR cycle represents a two-fold change.
Changes in mRNA abundance between samples were then determined from the ratio of the target gene Cq to the reference gene Cq.
The genes differentially expressed between normal and tumor samples were then identified using negative binomial test as stated in the DESeq package [ 15].
Differentially expressed genes between healthy and tumor samples were then identified using an empirical Bayes moderated t-test and adjusting P values with a false discovery rate of 5%.
Samples were then compared between tumors and nontumor controls using one-way ANOVA.
Technical replicates for cell line and human samples were then assessed between SAMs.
Fasting blood samples were then obtained between 8 00 and 10 00 A.M. to measure serum total testosterone (TT), estradiol (E2), sex hormone binding globuline (SHBG), luteinizing hormone (LH), follicle-stimulating hormone (FSH), prolactin (PRL), fasting plasma glucose (FPG), and HbA1c.
The samples were then aged for between 6 and 8 days at (295±3) K before analysis or gel preparation.
Samples were then submitted to heat treatments in air between 200 and 600 °C.
