The 5-year survival rate based on pathologic (p) stages was analysed using a large population of Japanese lung cancer cases (n=13 010) in 2005 (Asamura et al, 2008).
Data collected for the second stage were analysed using the least squares method which were applied to find the coefficients of a second order regression model.
Monomeric sugars from analysis of the raw material and the solids obtained from the pretreatment stage were analysed using by high-performance anion exchange chromatography coupled with pulsed amperometric detection (HPAEC-PAD).
The association of F17-related fimbriae, S and P fimbriae (grouped together), cytotoxic necrotising factors 1 and 2 (CNF1 and CNF2), aerobactin, TraT, and serum resistance with clinical course of mastitis, NAGase activity, and lactation stage were analysed using the Fisher's exact test, ANOVA, and Pearson's chi square test, respectively.
Change in CKD stage was analysed using the Mantel–Haenszel chi-squared test.
To gain a broad view on the transcriptional changes occurring during nodule development, the M. truncatula transcriptome at different nodulation stages was analysed using Mt16kOLI1Plus microarrays, which carry 16,470 M. truncatula probes [29], [30].
To investigate whether GalNAc-T3 expression level is significantly correlated with recurrence in early-stage diseases, disease-free survival curves of the patients with GalNAc-T3 expression in stage I were analysed using the Kaplan Meier method.
Blood samples from 58 MM patients (stage I IV) were analysed, using RT-PCR assay to detect tyrosinase mRNA.
Pooled serum from 10 individuals without cancer, early-stage gastric cancer (10 individuals, stages I II) and late-stage gastric cancer (10 individuals, stages III IV) were analysed using an array of antibodies to 36 cytokines.
The different stages of inbreeding were analysed using restriction fragment polymorphism, microsatellite variability and amplified fragment length polymorphism.
