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Graph prism 5

Manufactured by GraphPad
Sourced in United States

GraphPad Prism 5 is a comprehensive data analysis and graphing software. It provides a wide range of statistical analysis tools and versatile graphing capabilities to visualize and interpret scientific data.

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85 protocols using graph prism 5

1

Scratch Wound Assay for Cell Migration

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Cells were seeded on 24-well plates and incubated until reaching approximately 80% confluence. The cell surfaces were scratched with 200 μL sterile tip followed by PBS rinsing to remove debris. Cells were treated with ACN at the dose shown to inhibit cell viability by 50% (IC50) in 10% FBS-supplemented culture medium. Cell migration to the wounded area was assessed after 48 h through microphotographs from random fields (n ≥ 3) taken with a Keyence BZ-X710 Microscope (40X). The number of cells that migrated towards the wounded area were quantified using ImageJ software (http://imagej.nih.gov/ij/ accessed on 1 February 2020). Data from at least three independent experiments were analyzed with Graph Prism 5.0 (San Diego, CA, USA).
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2

Statistical Analysis of Experimental Data

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All statistical computations were performed using the Graph Prism 5.0 software (San Diego, CA, USA). Cox regression was performed with SPSS version 19.0 (SPSS, Inc., Chicago, IL, USA). Comparison of means in normally distributed data was performed using Students’ t test otherwise the nonparametric Mann-Whitney U test was applied or as stated. P-values of equal or less than 0.05 were considered statistically significant. All bar graphs are depicted using means and standard deviations as error bars, unless stated otherwise.
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3

Statistical Analysis of Cytokine Profiles

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Demographic and clinical characteristics were compared among subgroups by Mann–Whitney U test for continuous variables and χ2 test for categorical variables. The cytokine concentrations were expressed in pg/ml and were compared among groups using the Kruskal-Wallis followed by Dunn's posttest. Correlation coefficients were calculated with Pearson's test when the data had a normal distribution and with Spearman's when they had no normal distribution. A receiver-operating characteristic curve was made. Results were analyzed using GraphPRISM 5.0, and significant differences were considered at P < 0.05.
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4

Paw Volume Measurement Analysis

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The results are presented as the mean ± standard error mean (S.E.M.). Two-way ANOVA followed by Bonferroni's post hoc test was used to analyze paw volumes differences, with P values of < 0.05 considered significant. Statistical analyses were performed by using GraphPrism 5.0 (San Diego, USA) for Windows.
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5

Statistical Analyses in Biomedical Research

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Statistical analyses were performed using SPSS version 20.0 and Graph prism 5.0. Results are expressed as mean ± SE of the mean for normally distributed data. Inter-group comparisons for body weights were performed using one-way ANOVA with correction for multiple comparisons by Tukey’s post hoc test; P < 0.05 was considered statistically different. Inter-group comparisons of ACF counts and tumor measurements were assessed with the 2 × 2 factorial designs; P < 0.05 was regarded as statistically significant for each main effect and interaction.
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6

Neuroanatomical sex differences analysis

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Variables were described as mean ± standard deviation (SD). Normal distribution was assessed using the Anderson-Darling test, and unpaired t-tests were used to compare OB weights and number of cells and neurons between sex groups, since the distribution proved to be normal. Because the ratio between non-neuronal over neuronal numbers for females were not normally distributed, the Mann-Whitney test was used in this case. The same was done for the male group, since the number of cases did not allow proper application of the Anderson-Darling test. Statistical analysis was performed with the Graph Prism 5.0 software. All tests had the significance level set at 0.05.
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7

Comparative Analysis of Cell Viability

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For test, at least three replicates were performed. Data is shown as mean ± SEM. Among groups, significant differences were tested using Student’s t-test or one-way analysis of variance (ANOVA) coupled Tukey HSD multiple test. P < 0.05 was considered as significant. Graphs and charts were plotted using R 3.1 or Graphprism 5.0.
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8

Comparative Analysis of Gene Expression

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Comparisons were performed using the Wilcoxon–Mann–Whitney test (for two groups) and Student's t Test for paired samples showing normal distribution. Survival analyses (recurrence free or tumor progression in recurrence) according to various variables were performed using the Kaplan– Meyer method and differences between the patient groups were tested by the log-rank test. Discrimination between samples showing increased or decreased gene expression was made using the median. Overlapping significance was monitored by exact F Fisher test. SPSS 17.0 and Graph prism 5.0 software were used.
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9

Evaluating HBV DNA Quantification Assays

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Statistical analyses were performed using SPSS software version 19.0 and Graph Prism 5.0. Pearson’s correlation coefficients and linear regression were used for correlation analysis. Bland-Altman tests were used to assess the agreement of the quantitative results of HBV DNA between the CTM, v2 assay or the Daan test and the in-house method.
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10

Cytokine Gene Expression in RABV Infection

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Cox proportional hazards were used to estimate lethality rate and hazard ratios (HR) between groups. Kruskal–Wallis with p < 0.05 as the significance level was chosen for evaluation of gene expression of cytokines/chemokines and the RABV N gene. Graph-Prism® 5.0 and Instat® softwares were used as analysis tools. Gene expression of cytokines/chemokines were first compared between treated and non-treated groups inoculated with the same variant, at the same period, 5 or 10 days p.i (ex: hv3 non-treated 5 days vs hv3 siRNA treated at 5 days); a second comparison was made between groups at the same condition, inoculated (with same viral variant) treated and non-treated but at different periods, 5 and 10 days (ex: hv2 siRNA treated at 5 days vs hv2 siRNA treated at 10 days).
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